urea has been researched along with omecamtiv mecarbil in 125 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (1.60) | 29.6817 |
2010's | 61 (48.80) | 24.3611 |
2020's | 62 (49.60) | 2.80 |
Authors | Studies |
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Teerlink, JR | 1 |
Cas, LD; Cotter, G; Gheorghiade, M; Metra, M; Sabbah, HN; Teerlink, JR; Zacà, V | 1 |
Abarzúa, P; Depre, C; Dhar, SK; Malik, FI; Morgans, DJ; Shen, YT; Vatner, SF; Zhao, X | 1 |
Campia, U; Gheorghiade, M; Nodari, S | 1 |
Fox, CJ; Kaye, AD; Liu, H; Zhang, S | 1 |
Leinwand, LA; Moss, RL | 1 |
Anderson, RL; Baliga, R; Brejc, K; Cox, DR; Elias, KA; Finer, JT; Garard, M; Godinez, G; Hartman, JJ; Kass, DA; Katori, T; Kawas, R; Kraynack, E; Lee, KH; Lenzi, D; Lu, PP; Malik, FI; Morgan, BP; Morgans, DJ; Muci, A; Niu, C; Pierce, DW; Pokrovskii, M; Qian, X; Rodriguez, H; Sakowicz, R; Shen, YT; Suehiro, I; Sueoka, SH; Sylvester, S; Tochimoto, T; Valdez, C; Vatner, SF; Wang, W | 1 |
Bers, DM; Harris, SP | 1 |
Malik, FI; Morgan, BP | 1 |
Dickstein, K | 1 |
Bee, R; Chen, MM; Clarke, CP; Elliott, L; Escandon, RD; Goldman, JH; Habibzadeh, MR; Lee, JH; Malik, FI; Saikali, KG; Schiller, NB; Teerlink, JR; Wolff, AA | 1 |
Clarke, CP; Cleland, JG; Francis, DP; Goldman, JH; Greenberg, BH; Lang, CC; Lee, JH; Malik, FI; Mayet, J; Mc Murray, JJ; Monaghan, M; Neyses, L; Nifontov, EM; Saikali, KG; Saltzberg, M; Senior, R; Shaburishvili, T; Teerlink, JR; Tsyrlin, VA; Wasserman, SM; Wolff, AA | 1 |
Asselbergs, FW; Doevendans, PA; Meijs, MF | 1 |
Ezekowitz, JA | 1 |
Fang, W; Ma, Y; Mou, T; Peng, C; Zhang, M; Zhang, X; Zhao, Z | 1 |
Albert, NM; Butler, J; Carson, PE; Collins, SP; Colvin-Adams, M; Dimarco, JP; Ezekowitz, JA; Fang, JC; Givertz, MM; Hernandez, AF; Hershberger, RE; Katz, SD; Krishnamani, R; Rogers, JG; Spertus, JA; Starling, RC; Stevenson, WG; Stough, WG; Sweitzer, NK; Tang, WH; Teerlink, JR; Walsh, MN; Westlake Canary, CA | 1 |
Pollesello, P | 1 |
Valentova, M; von Haehling, S | 1 |
Balligand, JL; Bauersachs, J; Clerk, A; De Windt, L; Heymans, S; Hilfiker-Kleiner, D; Hirsch, E; Iaccarino, G; Knöll, R; Leite-Moreira, AF; Lourenço, AP; Mayr, M; Tarone, G; Thum, T; Tocchetti, CG | 1 |
Ajtai, K; Burghardt, TP; Wang, Y | 1 |
Chen, MM; Chou, W; Eisenberg, P; Escandón, R; Greenberg, BH; Lee, JH; Malik, FI; Megreladze, I; Saikali, KG; Shaburishvili, T; Treshkur, T; Wasserman, SM; Wolff, AA | 1 |
Belknap, B; Forgacs, E; Liu, Y; White, HD; Winkelmann, DA | 1 |
Houdusse, AM; Pylypenko, O; Shima, A; Song, L; Sweeney, HL; Yang, Z | 1 |
Aksel, T; Choe Yu, E; Ruppel, KM; Spudich, JA; Sutton, S | 1 |
Chow, AT; Ma, P; Malik, FI; Vu, T; Wang, YM; Xiao, JJ | 1 |
Aasum, E; Bakkehaug, JP; Boardman, N; Engstad, ET; How, OJ; Kildal, AB; Larsen, TS; Myrmel, T; Næsheim, T; Rønning, L | 1 |
Li, BH; Ryba, DM; Solaro, RJ; Utter, MS; Wolska, BM | 1 |
dos Remedios, CG; Gresham, KS; Li, A; Mamidi, R; Stelzer, JE | 1 |
Forgacs, E; Miller, MT; Stock, AM; Winkelmann, DA | 1 |
Dorhout, B; Liu, LC; Teerlink, JR; van der Meer, P; Voors, AA | 1 |
Bezemer, JM; Correll, TL; Kennedy, MT; Roberts, SW; Subramanian, R; Walker, SD | 1 |
Alvarez, P; Banfield, C; Johnson, J; Malik, F; Monsalvo, ML; Palaparthy, R; Smith, B; Yan, L | 1 |
Cleland, JGF; Dickstein, K; Ezekowitz, JA; Felker, GM; Filippatos, GS; Kim, JB; Knusel, B; Lei, L; Malik, FI; McMurray, JJV; Metra, M; Ponikowski, P; Teerlink, JR; Wasserman, SM; Wolff, AA | 1 |
Broughton, KM; Henze, MP; Li, J; Lin, YH; Russell, B; Sanchez-Freire, V; Sarmah, E; Solaro, RJ; Warren, CM | 1 |
Butler, J; Hamo, CE; Moin, DS; Sackheim, J | 1 |
Anatchkova, M; Chau, D; Malik, FI; Oko-Osi, H; Patrick, DL; Spertus, J; Teerlink, JR; von Maltzahn, R; Wiklund, I | 1 |
Banyasz, T; Horvath, B; Kistamas, K; Magyar, J; Masuda, L; Nanasi, PP; Papp, Z; Szentandrassy, N; Vaczi, K | 1 |
Adams, KF; Cleland, JG; Ezekowitz, JA; Felker, GM; Goudev, A; Honarpour, N; Johnston, J; Macdonald, P; Malik, FI; McMurray, JJ; Metra, M; Mitrovic, V; Monsalvo, ML; Ponikowski, P; Serpytis, P; Solomon, SD; Spinar, J; Teerlink, JR; Tomcsányi, J; Vandekerckhove, HJ; Voors, AA | 1 |
Lim, GB | 1 |
Blair, CA; Campbell, KS; Fetrow, CM; Previs, MJ; Swenson, AM; Tang, W; Unrath, WC; Yengo, CM | 1 |
Muretta, JM; Rohde, JA; Thomas, DD | 1 |
Psotka, MA; Teerlink, JR | 1 |
Almássy, J; Gaburjakova, J; Gaburjakova, M; Nánási, P | 1 |
Hartman, JJ; Houdusse, A; Malik, FI; Planelles-Herrero, VJ; Robert-Paganin, J | 1 |
Chandra, M; Gollapudi, SK; Reda, SM | 1 |
Chien, FJ; Eisen, HJ; Kim, DH | 1 |
Almássy, J; Bányász, T; Horváth, B; Magyar, J; Nánási, PP; Papp, Z; Szentandrássy, N; Tóth, A; Veress, R | 1 |
Irving, M; Kampourakis, T; Sun, YB; Zhang, X | 1 |
Fornili, A; Hashem, S; Tiberti, M | 1 |
Almassy, J; Gaburjakova, M; Komaromi, I; Nanasi, P | 1 |
Annoni, F; El-Oumeiri, B; Herpain, A; Jespers, P; Mc Entee, K; van de Borne, P; Van Nooten, G; Vanden Eynden, F | 1 |
Almássy, J; Komáromi, I; Nánási, P | 1 |
Kawana, M; Liu, C; Ruppel, KM; Song, D; Spudich, JA | 1 |
Barua, B; Goldman, YE; Greenberg, MJ; Ostap, EM; Winkelmann, DA; Woody, MS | 1 |
Anker, SD; Balligand, JL; Bauersachs, J; Brutsaert, D; Carrier, L; Chlopicki, S; Cleland, JG; de Boer, RA; de Keulenaer, G; Dietl, A; Eschenhagen, T; Fischmeister, R; Hamdani, N; Harjola, VP; Heinzel, FR; Heymans, S; Hilfiker-Kleiner, D; Holzmeister, J; Limongelli, G; Linke, WA; Lund, LH; Lyon, AR; Maack, C; Manstein, DJ; Masip, J; Mebazaa, A; Metra, M; Metzger, J; Mueller, C; Papp, Z; Pieske, B; Ponikowski, P; Ristić, A; Ruschitzka, F; Seferović, PM; Skouri, H; Tocchetti, CG; Yilmaz, MB; Zimmermann, WH | 1 |
Bakkehaug, JP; How, OJ; Kildal, AB; Myrmel, T; Rødland, L; Rønning, L | 1 |
Agarwal, R; Chen, CS; Chopra, A; Cicconet, M; Ewoldt, J; Garfinkel, AC; Mücke, M; Neyazi, M; Pourquié, O; Rao, J; Schmid, M; Seidman, CE; Seidman, JG; Sharma, A; Toepfer, CN; Willcox, JAL | 1 |
Seidman, CE; Seidman, JG; Yotti, R | 1 |
Awinda, PO; Kieu, TT; Tanner, BCW | 1 |
Bauersachs, J; Berliner, D | 1 |
Desetty, R; Tang, W; Unrath, WC; Yengo, CM | 1 |
How, OJ; Kildal, AB; Myrmel, T; Rødland, L; Rønning, L | 1 |
Aghdam, RM; Emami, SH; Kiaie, N; Rabbani, S; Tafti, HA | 1 |
Granzier, H; Karimi, E; Kolb, J; Lee, EJ; Lindqvist, J | 1 |
Lüscher, TF | 1 |
Braren, I; Denning, C; Eschenhagen, T; Hansen, A; Mannhardt, I; Saleem, U | 1 |
Büchele, G; Diaz, R; Felker, GM; Honarpour, N; Kurtz, CE; Legg, JC; Malik, FI; McMurray, JJV; Metra, M; Solomon, SD; Teerlink, JR; Varin, C | 1 |
Berg, VY; Bershitsky, SY; Kochurova, AM; Kopylova, GV; Nabiev, SR; Nikitina, LV; Shchepkin, DV | 1 |
Mehmood, M | 1 |
Caremani, M; Gallart, C; Governali, S; Linari, M; Lombardi, V; Ottenheijm, C; Pertici, I; Piazzesi, G; Stienen, G | 1 |
Ballan, N; Gepstein, L; Keller, GM; Shaheen, N | 1 |
Gao, B; Qu, Y; Sutherland, W; Vargas, HM | 1 |
Abbasi, SA; Adams, KF; Anand, I; Arias-Mendoza, A; Biering-Sørensen, T; Böhm, M; Bonderman, D; Cleland, JGF; Corbalan, R; Crespo-Leiro, MG; Dahlström, U; Diaz, R; Echeverria Correa, LE; Fang, JC; Felker, GM; Filippatos, G; Fonseca, C; Goncalvesova, E; Goudev, AR; Howlett, JG; Kurtz, CE; Lanfear, DE; Legg, JC; Lund, M; Macdonald, P; Malik, FI; Mareev, V; McMurray, JJV; Metra, M; Momomura, SI; O'Meara, E; Parkhomenko, A; Ponikowski, P; Ramires, FJA; Serpytis, P; Sharpsten, L; Sliwa, K; Solomon, SD; Spinar, J; Suter, TM; Teerlink, JR; Tomcsanyi, J; Vandekerckhove, H; Varin, C; Vinereanu, D; Voors, AA; Yilmaz, MB; Zannad, F | 1 |
Bernier, TD; Buckley, LF | 1 |
Abbasi, SA; Cleland, JGF; Felker, GM; Globe, G; Malik, FI; McMurray, JJV; Solomon, SD; Teerlink, JR; Zhang, H | 1 |
Abbasi, S; Biering-Sørensen, T; Claggett, B; Felker, GM; Kurtz, CE; Liu, J; Malik, FI; McMurray, JJV; Minamisawa, M; Solomon, SD; Teerlink, JR | 1 |
Abbasi, SA; Adams, KF; Anand, I; Arias-Mendoza, A; Biering-Sørensen, T; Böhm, M; Bonderman, D; Cleland, JGF; Corbalan, R; Crespo-Leiro, MG; Dahlström, U; Diaz, R; Echeverria, LE; Fang, JC; Felker, GM; Filippatos, G; Fonseca, C; Goncalvesova, E; Goudev, AR; Honarpour, N; Howlett, JG; Kurtz, CE; Lanfear, DE; Legg, JC; Li, J; Lund, M; Macdonald, P; Malik, FI; Mareev, V; McMurray, JJV; Metra, M; Momomura, SI; O'Meara, E; Parkhomenko, A; Ponikowski, P; Ramires, FJA; Serpytis, P; Sharpsten, L; Sliwa, K; Solomon, SD; Spinar, J; Suter, TM; Teerlink, JR; Tomcsanyi, J; Vandekerckhove, H; Varin, C; Vinereanu, D; Voors, AA; Yilmaz, MB; Zannad, F | 1 |
Swedberg, K | 1 |
Carlo, P; Massimo, V | 1 |
Lam, CSP; Teramoto, K; Tromp, J | 1 |
Atherton, JL; Barua, B; Forgacs, E; Goldman, YE; Ostap, EM; Shuman, H; Snoberger, A; Winkelmann, DA | 1 |
Doh, CY; Dominic, KL; Holmes, JB; Madugula, N; Mamidi, R; Stelzer, JE | 1 |
Ali, A; Ikram, S; Shah, SR | 1 |
Biering-Sørensen, T; Claggett, B; Felker, GM; Honarpour, N; Kurtz, CE; Legg, JC; Liu, J; Malik, FI; McMurray, JJV; Minamisawa, M; Papolos, AI; Solomon, SD; Teerlink, JR | 1 |
Kumar, P; Palaian, S; Prabhu, MM | 1 |
Beard, N; Chan, W; Cheesman, E; Dashwood, A; Haqqani, H; Hay, K; Molenaar, P; Spratt, M; Wong, YW | 1 |
Arimura, Z; Fang, M; Gao, B; Qu, Y; Vargas, HM | 1 |
Felker, GM; Mann, DL | 1 |
Campbell, SG; Sewanan, LR; Shen, S | 1 |
Komamura, K | 1 |
Bonapace, S; Molon, G | 1 |
Bellumkonda, L | 1 |
Felker, GM; McMurray, JJV; Teerlink, JR | 1 |
Dutta, S; Lee, E; Mackowski, M; Trivedi, A; Wahlstrom, J | 1 |
Abbasi, SA; Biering-Sørensen, T; Böhm, M; Bonderman, D; Claggett, BL; Diaz, R; Fang, JC; Felker, GM; Flores-Arredondo, JH; Heitner, SB; Kupfer, S; Lanfear, DE; Lund, M; Malik, FI; McMurray, JJV; Metra, M; Momomura, SI; O'Meara, E; Ponikowski, P; Solomon, SD; Spinar, J; Teerlink, JR | 1 |
Ferreira, JP | 1 |
Gronda, E; Iacoviello, M; Palazzuoli, A | 1 |
Abbasi, S; Dutta, S; Flach, S; Jafarinasabian, P; Lee, E; Mackowski, M; Oberoi, RK; Simiens, MA; Terminello, B; Trivedi, A; Zhang, H | 1 |
Campbell, SG; Jacoby, DL; Sewanan, LR; Shen, S | 1 |
Abbasi, S; Dutta, S; Flach, S; Jafarinasabian, P; Lee, E; Oberoi, RK; Spring, M; Trivedi, A; Zhang, H | 1 |
Abbasi, S; Dutta, S; Flach, S; Hutton, S; Jafarinasabian, P; Lee, E; Mackowski, M; Oberoi, RK; Trivedi, A; Zhang, H | 1 |
Bhatia, A; Dutta, S; Flach, S; Jafarinasabian, P; Lee, E; Mackowski, M; Terminello, B; Trivedi, A; Zhang, H | 1 |
Abbasi, S; Brooks, A; Darpo, B; Dutta, S; Flach, S; Hsu, CP; Israel, S; Jafarinasabian, P; Lee, E; Terminello, B; Trivedi, A; Xue, H; Zhang, H | 1 |
Abbasi, S; Dutta, S; Flach, S; Jafarinasabian, P; Lee, E; Malik, FI; Trivedi, A; Zhang, H | 1 |
Chen, CH; Chen, YJ; Cheng, HM; Chiang, CE; Chien, CS | 1 |
Abbasi, S; Dutta, S; Flach, S; Jafarinasabian, P; Lee, E; Sohn, W; Terminello, B; Trivedi, A; Zhang, H | 1 |
Annoni, F; El Oumeiri, B; Herpain, A; Hubesch, G; Jespers, P; Mc Entee, K; Stefanidis, C; van de Borne, P; Vanden Eynden, F | 1 |
Abbasi, S; Aoki, M; Dutta, S; Hutton, S; Lee, E; Mackowski, M; Malik, FI; Trivedi, A | 1 |
Abbasi, S; Dutta, S; Flach, S; Jafarinasabian, P; Kulkarni, P; Lee, E; Sohn, W; Spring, M; Trivedi, A; Wahlstrom, J; Zhang, H | 1 |
Alothman, AA; Arumugam, R; Atallah, MM; Bagheri, D; Cui, M; El-Sabbagh, NM; El-Sayed, NS; Ghafarifarsani, H; Ghetas, HA; Hedayati, SA; Hosseini Shekarabi, SP; Inoue, Y; Khalil, RH; Khallaf, MM; Kuroda, Y; Kuznetsov, D; Lee, J; Lookin, O; Nam, YW; Nemoto, H; Nguyen, M; Noda, M; Numaguchi, R; Orfali, R; Priscillal, IJD; Protsenko, Y; Rahman, MA; Shahbazi Naserabad, S; Shakweer, MS; Sheikh Veisi, R; Takahashi, K; Tanaka, C; Wada, K; Wang, SF; Yang, G; Yoshino, K; Zhang, M | 1 |
Kravchenko, I; Medentseva, O; Rudyk, I | 1 |
Abbasi, S; Dutta, S; Flach, S; Hsu, CP; Hutton, S; Jafarinasabian, P; Lee, E; Sohn, W; Trivedi, A; Zhang, H | 1 |
Abbasi, SA; Anand, I; Claggett, B; Crespo-Leiro, MG; Dahlström, U; Diaz, R; Felker, GM; Goncalvesova, E; Heitner, SB; Howlett, JG; Hucko, T; Kupfer, S; MacDonald, P; Malik, FI; McMurray, JJV; Metra, M; Parkhomenko, A; Solomon, SD; Teerlink, JR; Tomcsányi, J | 1 |
Acero, JC; Butova, X; Gurev, V; Khamzin, S; Khokhlova, A; Kozloski, J; Myachina, T; Parikh, J; Rumbell, T; Solovyova, O | 1 |
Ahamadi, M; Chen, PW; Dutta, S; Lee, E; Trivedi, A | 1 |
Christ, T; Eschenhagen, T; Hansen, A; Pietsch, N; Rhoden, A; Schulze, T | 1 |
Chen, WJ; Huang, CH; Tsai, MS; Wu, SN | 1 |
Claggett, BL; Corbalan, R; Diaz, R; Felker, GM; Filippatos, G; Goudev, AR; Heitner, SB; Kupfer, S; Malik, FI; Mareev, V; McMurray, JJV; Metra, M; Miao, ZM; Serpytis, P; Solomon, SD; Suter, T; Teerlink, JR; Yilmaz, MB; Zannad, F | 1 |
Rienstra, M; van der Meer, P; van Veldhuisen, DJ | 1 |
Böhm, M; Cohen-Solal, A; Divanji, PH; Docherty, KF; Ezekowitz, JA; Felker, GM; Heitner, SB; Kupfer, S; Lewis, GD; Lopes, RD; Malik, FI; Meng, L; Metra, M; Teerlink, JR; Voors, AA; Whellan, DJ; Wohltman, A | 1 |
Drazner, MH | 1 |
Barge-Caballero, E; Crespo-Leiro, MG; McDonagh, TA | 1 |
Hernandez, AF | 1 |
Adams, KF; Anand, I; Badat, A; Burgess, L; Claggett, BL; Diaz, R; Fang, JC; Felker, GM; Gorodeski, EZ; Heitner, SB; Kupfer, S; Lanfear, DE; Malik, FI; McMurray, JJV; Metra, M; Miao, ZM; Njoroge, JN; Ramires, F; Sliwa-Hahnle, K; Solomon, S; Teerlink, JR; Williams, C | 1 |
Albert, NM; Alhanti, B; Allen, LA; DeVore, AD; Divanji, PH; Felker, GM; Fonarow, GC; Greene, SJ; Harrington, J; Heitner, SB; Sun, JL; Yancy, CW | 1 |
21 review(s) available for urea and omecamtiv mecarbil
Article | Year |
---|---|
A novel approach to improve cardiac performance: cardiac myosin activators.
Topics: Animals; Cardiac Myosins; Cardiotonic Agents; Clinical Trials, Phase I as Topic; Clinical Trials, Phase II as Topic; Heart Failure; Humans; Myocardial Contraction; Urea; Ventricular Function, Left | 2009 |
Agents with inotropic properties for the management of acute heart failure syndromes. Traditional agents and beyond.
Topics: Acute Disease; Cardiotonic Agents; Digoxin; Dobutamine; Etiocholanolone; Exercise Test; Heart Failure; Hemodynamics; Hospitals, Group Practice; Humans; Hydrazones; Prognosis; Pyrazines; Pyridazines; Quinolines; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Simendan; Treatment Outcome; Urea; Vasodilator Agents | 2009 |
Cardiovascular pharmacology: an update.
Topics: Animals; Cardiovascular Agents; Cardiovascular Diseases; Diastole; Heart Failure; Humans; Hydrazones; Muscle Contraction; Myofibrils; Natriuretic Peptide, Brain; Nicardipine; Pyridazines; Pyridines; Sarcomeres; Simendan; Urea | 2010 |
Cardiac myosin activation part 1: from concept to clinic.
Topics: Animals; Cardiotonic Agents; Clinical Trials, Phase II as Topic; Drug Evaluation, Preclinical; Heart Failure, Systolic; Humans; Myocardial Contraction; Myocardium; Myosins; Small Molecule Libraries; Urea | 2011 |
Novel pharmacologic therapies in development for acute decompensated heart failure.
Topics: Acute Disease; Atrial Natriuretic Factor; Diuretics; Heart Failure; Humans; Peptide Fragments; Relaxin; Urea; Vasodilator Agents | 2013 |
Acute decompensated heart failure: update on new and emerging evidence and directions for future research.
Topics: Adrenomedullin; Atrial Natriuretic Factor; Biomarkers; Blood Pressure Monitoring, Ambulatory; Cardiotonic Agents; Clinical Trials as Topic; Diet, Sodium-Restricted; Diuretics; Dopamine; Dose-Response Relationship, Drug; Dyspnea; Glycopeptides; Heart Failure; Hemofiltration; Hospitalization; Humans; Natriuretic Agents; Natriuretic Peptide, Brain; Nitroglycerin; Peptide Fragments; Prognosis; Protein Precursors; Quality of Health Care; Relaxin; Risk Assessment; Saline Solution, Hypertonic; Urea; Vasodilator Agents; Xanthines | 2013 |
An overview of recent developments in the treatment of heart failure: update from the ESC Congress 2013.
Topics: Amides; Benzoates; Cardiac Resynchronization Therapy; Cardiotonic Agents; Fumarates; Heart Failure; Humans; Recombinant Proteins; Relaxin; Ultrafiltration; Urea | 2014 |
Targeting myocardial remodelling to develop novel therapies for heart failure: a position paper from the Working Group on Myocardial Function of the European Society of Cardiology.
Topics: Cell Survival; Cyclosporine; Drugs, Investigational; Heart Failure; Humans; Hypertrophy, Left Ventricular; Myocardial Contraction; Myocytes, Cardiac; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Translational Research, Biomedical; Urea; Ventricular Remodeling | 2014 |
Omecamtiv mecarbil: a new cardiac myosin activator for the treatment of heart failure.
Topics: Animals; Cardiac Myosins; Cardiotonic Agents; Disease Models, Animal; Heart Failure, Systolic; Humans; Myocardial Contraction; Randomized Controlled Trials as Topic; Urea | 2016 |
Manufacturing of [(14)C]-Labeled Drug Substance and Drug Product Utilized in Clinical Research: A Case Study of Omecamtiv Mecarbil.
Topics: Absorption, Physiological; Carbon Radioisotopes; Clinical Trials as Topic; Drug Compounding; Drug Liberation; Humans; Urea | 2016 |
Cardiac Myosin Activators in Systolic Heart Failure: More Friend than Foe?
Topics: Animals; Cardiac Myosins; Cardiotonic Agents; Disease Models, Animal; Heart Failure, Systolic; Humans; Myocardial Contraction; Randomized Controlled Trials as Topic; Stroke Volume; Urea | 2016 |
Direct Myosin Activation by Omecamtiv Mecarbil for Heart Failure with Reduced Ejection Fraction.
Topics: Animals; Cardiac Myosins; Cardiotonic Agents; Clinical Trials as Topic; Disease Models, Animal; Heart Failure; Humans; Myocardial Contraction; Stroke Volume; Urea | 2017 |
Pharmacologic Management for Heart Failure and Emerging Therapies.
Topics: Aminobutyrates; Benzazepines; Benzhydryl Compounds; Biphenyl Compounds; Cardiovascular Agents; Drug Combinations; Glucosides; Heart Failure; Humans; Ivabradine; Neuregulin-1; Recombinant Proteins; Relaxin; Stroke Volume; Tetrazoles; Urea; Valsartan | 2017 |
Omecamtiv Mecarbil: A Myosin Motor Activator Agent with Promising Clinical Performance and New in vitro Results.
Topics: Animals; Cardiotonic Agents; Dose-Response Relationship, Drug; Enzyme Activators; Heart Failure; Humans; Myocardial Contraction; Myosins; Oxygen Consumption; Ryanodine Receptor Calcium Release Channel; Urea | 2018 |
Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies.
Topics: Benzylamines; Cardiac Myosins; Cardiomyopathy, Dilated; Cardiomyopathy, Hypertrophic; Cardiotonic Agents; Carrier Proteins; Connectin; Gene Expression; Humans; Mutation; Myocardial Contraction; Myocardium; Myosin Heavy Chains; RNA-Binding Proteins; Sarcomeres; Troponin T; Uracil; Urea | 2019 |
New drugs: big changes in conservative heart failure therapy?
Topics: Adrenergic beta-Antagonists; Algorithms; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Benzhydryl Compounds; Cardiac Glycosides; Cardiotonic Agents; Diuretics; Enzyme Activators; Glucosides; Heart Failure; Humans; Hyperkalemia; Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels; Iron; Ivabradine; Mineralocorticoid Receptor Antagonists; Neprilysin; Practice Guidelines as Topic; Pyrazoles; Pyrimidines; Renin; Renin-Angiotensin System; Sodium-Glucose Transporter 2 Inhibitors; Stroke Volume; Urea | 2019 |
Omecamtiv Mecarbil in Chronic Heart Failure With Reduced Ejection Fraction: Rationale and Design of GALACTIC-HF.
Topics: Heart Failure; Humans; Myocardial Contraction; Randomized Controlled Trials as Topic; Stroke Volume; Urea; Ventricular Function, Left | 2020 |
Cardiac Myosin Activation for the Treatment of Systolic Heart Failure.
Topics: Animals; Cardiac Myosins; Cardiotonic Agents; Heart Failure, Systolic; Humans; Myocardium; Recovery of Function; Signal Transduction; Stroke Volume; Treatment Outcome; Urea; Ventricular Dysfunction, Left; Ventricular Function, Left; Ventricular Remodeling | 2021 |
Mechanisms and Models in Heart Failure: A Translational Approach.
Topics: Aminobutyrates; Angiotensin Receptor Antagonists; Biphenyl Compounds; Clinical Trials, Phase III as Topic; Drug Combinations; Drug Development; Enzyme Activators; Heart Failure; Heterocyclic Compounds, 2-Ring; Humans; Models, Biological; Natriuretic Peptides; Neprilysin; Pyrimidines; Sodium-Glucose Transporter 2 Inhibitors; Soluble Guanylyl Cyclase; Stroke Volume; Urea; Valsartan; Ventricular Remodeling | 2021 |
Recent advances in pharmacological treatment of heart failure.
Topics: Aminobutyrates; Angiotensin Receptor Antagonists; Biphenyl Compounds; Cardiotonic Agents; Drug Combinations; Ferric Compounds; Heart Failure; Heterocyclic Compounds, 2-Ring; Hospitalization; Humans; Iron Deficiencies; Maltose; Pyrimidines; Sodium-Glucose Transporter 2 Inhibitors; Stroke Volume; Urea; Valsartan; Vasodilator Agents; Ventricular Remodeling | 2021 |
From Genetic Mutations to Molecular Basis of Heart Failure Treatment: An Overview of the Mechanism and Implication of the Novel Modulators for Cardiac Myosin.
Topics: Benzylamines; Cardiac Myosins; Heart Failure; Humans; Molecular Targeted Therapy; Myocytes, Cardiac; Uracil; Urea | 2021 |
22 trial(s) available for urea and omecamtiv mecarbil
Article | Year |
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Dose-dependent augmentation of cardiac systolic function with the selective cardiac myosin activator, omecamtiv mecarbil: a first-in-man study.
Topics: Adult; Cardiac Myosins; Cross-Over Studies; Dose-Response Relationship, Drug; Double-Blind Method; Humans; Infusions, Intravenous; Male; Maximum Tolerated Dose; Middle Aged; Myocardial Contraction; Stroke Volume; Systole; Urea; Ventricular Function, Left; Young Adult | 2011 |
The effects of the cardiac myosin activator, omecamtiv mecarbil, on cardiac function in systolic heart failure: a double-blind, placebo-controlled, crossover, dose-ranging phase 2 trial.
Topics: Blood Pressure; Cardiac Myosins; Cross-Over Studies; Double-Blind Method; Echocardiography; Female; Heart Failure, Systolic; Humans; Infusions, Intravenous; Male; Stroke Volume; Systole; Urea; Ventricular Dysfunction, Left | 2011 |
Safety and tolerability of omecamtiv mecarbil during exercise in patients with ischemic cardiomyopathy and angina.
Topics: Administration, Oral; Adult; Aged; Aged, 80 and over; Angina Pectoris; Dose-Response Relationship, Drug; Double-Blind Method; Drug Tolerance; Exercise; Exercise Test; Female; Follow-Up Studies; Georgia (Republic); Humans; Male; Middle Aged; Myocardial Contraction; Myocardial Ischemia; Retrospective Studies; Russia; Treatment Outcome; Urea | 2015 |
Population pharmacokinetic-pharmacodynamic modeling of omecamtiv mecarbil, a cardiac myosin activator, in healthy volunteers and patients with stable heart failure.
Topics: Adult; Aged; Cardiac Myosins; Cross-Over Studies; Double-Blind Method; Female; Healthy Volunteers; Heart Failure; Humans; Male; Middle Aged; Models, Biological; Stroke Volume; Systole; Urea; Young Adult | 2015 |
Relative bioavailability, food effect, and safety of the single-dose pharmacokinetics of omecamtiv mecarbil following administration of different modified-release formulations in healthy subjects.
Topics: Adolescent; Adult; Area Under Curve; Biological Availability; Chemistry, Pharmaceutical; Cross-Over Studies; Female; Food-Drug Interactions; Humans; Male; Middle Aged; Urea | 2016 |
Acute Treatment With Omecamtiv Mecarbil to Increase Contractility in Acute Heart Failure: The ATOMIC-AHF Study.
Topics: Acute Disease; Adolescent; Adult; Aged; Aged, 80 and over; Dose-Response Relationship, Drug; Double-Blind Method; Echocardiography; Female; Follow-Up Studies; Heart Failure; Heart Ventricles; Humans; Infusions, Intravenous; Male; Middle Aged; Myocardial Contraction; Prospective Studies; Stroke Volume; Treatment Outcome; Troponin; Urea; Ventricular Function, Left; Young Adult | 2016 |
Chronic Oral Study of Myosin Activation to Increase Contractility in Heart Failure (COSMIC-HF): a phase 2, pharmacokinetic, randomised, placebo-controlled trial.
Topics: Administration, Oral; Cardiac Myosins; Dose-Response Relationship, Drug; Heart Failure; Humans; Natriuretic Peptide, Brain; Peptide Fragments; Stroke Volume; Systole; Urea; Ventricular Function, Left; Ventricular Remodeling | 2016 |
Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction: GALACTIC-HF baseline characteristics and comparison with contemporary clinical trials.
Topics: Aged; Female; Heart Failure; Humans; Male; Middle Aged; Randomized Controlled Trials as Topic; Stroke Volume; Urea; Ventricular Function, Left | 2020 |
Effects of Omecamtiv Mecarbil on Symptoms and Health-Related Quality of Life in Patients With Chronic Heart Failure: Results From the COSMIC-HF Study.
Topics: Aged; Biomarkers; Chronic Disease; Female; Heart Failure; Humans; Male; Middle Aged; Patient Reported Outcome Measures; Quality of Life; Severity of Illness Index; Stroke Volume; Surveys and Questionnaires; Urea; Ventricular Dysfunction, Left | 2020 |
Cardiac Myosin Activator Omecamtiv Mecarbil Improves Left Ventricular Myocardial Deformation in Chronic Heart Failure: The COSMIC-HF Trial.
Topics: Aged; Biomarkers; Double-Blind Method; Female; Heart Failure; Heart Rate; Humans; Male; Middle Aged; Systole; Urea; Ventricular Dysfunction, Left; Ventricular Remodeling | 2020 |
Cardiac Myosin Activation with Omecamtiv Mecarbil in Systolic Heart Failure.
Topics: Aged; Aged, 80 and over; Cardiac Myosins; Cardiotonic Agents; Cardiovascular Diseases; Female; Heart Failure, Systolic; Humans; Male; Middle Aged; Myocardial Contraction; Stroke Volume; Urea | 2021 |
Pharmacokinetics, Disposition, and Biotransformation of [
Topics: Administration, Intravenous; Administration, Oral; Adult; Biological Availability; Biotransformation; Cardiovascular Agents; Cytochrome P450 Family 4; Healthy Volunteers; Heart Failure; Hepatobiliary Elimination; Humans; Infusions, Intravenous; Intestinal Absorption; Male; Renal Elimination; Urea | 2021 |
Effect of Ejection Fraction on Clinical Outcomes in Patients Treated With Omecamtiv Mecarbil in GALACTIC-HF.
Topics: Aged; Female; Heart Failure; Humans; Male; Middle Aged; Stroke Volume; Treatment Outcome; Urea | 2021 |
Switchability and minimal effect of food on pharmacokinetics of modified release tablet strengths of omecamtiv mecarbil, a cardiac myosin activator.
Topics: Administration, Oral; Adult; Area Under Curve; Cardiac Myosins; Cross-Over Studies; Delayed-Action Preparations; Drug Substitution; Fasting; Female; Food-Drug Interactions; Healthy Volunteers; Humans; Male; Middle Aged; Tablets; Therapeutic Equivalency; Urea | 2021 |
Relative Bioavailability of Omecamtiv Mecarbil Pediatric Minitablet Formulations in Healthy Adult Subjects.
Topics: Administration, Oral; Adolescent; Adult; Biological Availability; Cross-Over Studies; Delayed-Action Preparations; Drug Compounding; Female; Half-Life; Healthy Volunteers; Heart Failure; Humans; Male; Middle Aged; Myalgia; Tablets; Urea; Young Adult | 2021 |
Omecamtiv mecarbil does not prolong QTc intervals at therapeutic concentrations.
Topics: Cross-Over Studies; Double-Blind Method; Electrocardiography; Fluoroquinolones; Heart Rate; Humans; Moxifloxacin; Urea | 2022 |
Pharmacokinetics, Tolerability, and Safety of Single and Multiple Omecamtiv Mecarbil Doses in Healthy Japanese and Caucasian Subjects.
Topics: Administration, Oral; Adult; Area Under Curve; Asian People; Biological Availability; Female; Half-Life; Healthy Volunteers; Humans; Japan; Male; Tablets; Urea | 2021 |
Topics: Aeromonas hydrophila; Animal Feed; Animals; Antioxidants; Cadmium Chloride; Calmodulin; Cardiotonic Agents; Carps; Cichlids; Diet; Dietary Supplements; Dose-Response Relationship, Drug; Fish Diseases; Heart; Heart Failure; Lacticaseibacillus casei; Liver; Magnetic Iron Oxide Nanoparticles; Male; Monocrotaline; Mutagenesis, Site-Directed; Myocardial Contraction; Oxidative Stress; Potassium Channels, Calcium-Activated; Rats; Rats, Wistar; Urea; Withania | 2021 |
Assessment of Omecamtiv Mecarbil for the Treatment of Patients With Severe Heart Failure: A Post Hoc Analysis of Data From the GALACTIC-HF Randomized Clinical Trial.
Topics: Blood Pressure; Double-Blind Method; Female; Heart Failure; Humans; Male; Middle Aged; Patient Acuity; Retrospective Studies; Stroke Volume; Treatment Outcome; Urea; Ventricular Function, Left | 2022 |
Influence of atrial fibrillation on efficacy and safety of omecamtiv mecarbil in heart failure: the GALACTIC-HF trial.
Topics: Atrial Fibrillation; Atrial Flutter; Digoxin; Heart Failure; Humans; Quality of Life; Stroke Volume; Urea; Ventricular Function, Left | 2022 |
Effect of Omecamtiv Mecarbil on Exercise Capacity in Chronic Heart Failure With Reduced Ejection Fraction: The METEORIC-HF Randomized Clinical Trial.
Topics: Aged; Cardiovascular Agents; Chronic Disease; Double-Blind Method; Exercise Tolerance; Female; Heart Failure; Humans; Male; Middle Aged; Stroke Volume; Urea; Ventricular Dysfunction, Left; Ventricular Function, Left | 2022 |
Omecamtiv Mecarbil in Black Patients With Heart Failure and Reduced Ejection Fraction: Insights From GALACTIC-HF.
Topics: Heart Failure; Humans; Stroke Volume; Urea; Ventricular Function, Left | 2023 |
82 other study(ies) available for urea and omecamtiv mecarbil
Article | Year |
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Improvement of cardiac function by a cardiac Myosin activator in conscious dogs with systolic heart failure.
Topics: Analysis of Variance; Animals; Cardiac Myosins; Consciousness; Disease Models, Animal; Dobutamine; Dogs; Drug Administration Schedule; Female; Heart Failure, Systolic; Heart Function Tests; Infusions, Intravenous; Male; Myocardial Contraction; Myocardial Infarction; Oxygen Consumption; Probability; Random Allocation; Stroke Volume; Treatment Outcome; Urea; Ventricular Function, Left; Ventricular Remodeling | 2010 |
Acute heart failure with low cardiac output: can we develop a short-term inotropic agent that does not increase adverse events?
Topics: Acute Disease; Animals; Cardiac Output; Cardiotonic Agents; Clinical Trials as Topic; Digoxin; Dobutamine; Etiocholanolone; Genetic Therapy; Heart Failure; Humans; Hydrazones; Pyridazines; Ryanodine Receptor Calcium Release Channel; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Simendan; Sodium-Potassium-Exchanging ATPase; Urea | 2010 |
Medicine. Chemically tuned myosin motors.
Topics: Actins; Adenosine Diphosphate; Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Cardiac Myosins; Heart Failure, Systolic; Humans; Myocardial Contraction; Phosphates; Protein Binding; Protein Isoforms; Urea | 2011 |
Cardiac myosin activation: a potential therapeutic approach for systolic heart failure.
Topics: Actin Cytoskeleton; Actins; Adenosine Triphosphatases; Adenosine Triphosphate; Adrenergic beta-Agonists; Allosteric Regulation; Animals; Binding Sites; Calcium; Cardiac Myosins; Cardiac Output; Dogs; Female; Heart Failure, Systolic; Isoproterenol; Male; Myocardial Contraction; Myocytes, Cardiac; Phosphates; Protein Binding; Protein Conformation; Protein Isoforms; Rats; Rats, Sprague-Dawley; Urea; Ventricular Function, Left | 2011 |
Translational medicine: to the rescue of the failing heart.
Topics: Cardiotonic Agents; Heart; Heart Failure; Humans; Translational Research, Biomedical; Urea | 2011 |
Cardiac myosin activation: will theory and practice coincide?
Topics: Cardiac Myosins; Heart Failure, Systolic; Humans; Urea | 2011 |
Omecamtiv mecarbil: a promising new drug in systolic heart failure.
Topics: Heart Failure, Systolic; Humans; Muscle Cells; Myosins; Urea; Ventricular Function, Left | 2012 |
Synthesis and 18F-labeling of the analogues of Omecamtiv Mecarbil as a potential cardiac myosin imaging agent with PET.
Topics: Animals; Cattle; Chemical Phenomena; Chemistry Techniques, Synthetic; Drug Stability; Fluorine Radioisotopes; Isotope Labeling; Mice; Myocardium; Myosins; Positron-Emission Tomography; Radiochemistry; Substrate Specificity; Urea | 2013 |
Drug discovery and development for acute heart failure drugs: are expectations too high?
Topics: Acute Disease; Cardiotonic Agents; Clinical Trials as Topic; Drug Discovery; Heart Failure; Humans; Hydrazones; Pyridazines; Simendan; Urea | 2014 |
Analytical comparison of natural and pharmaceutical ventricular myosin activators.
Topics: Adenosine Triphosphatases; Animals; Muscle, Skeletal; Myocardium; Quantum Dots; Rabbits; Streptavidin; Urea; Ventricular Myosins | 2014 |
Omecamtiv Mecarbil modulates the kinetic and motile properties of porcine β-cardiac myosin.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Animals; Cardiac Myosins; Kinetics; Myocardial Contraction; Myocardium; Swine; Urea | 2015 |
Myosin VI deafness mutation prevents the initiation of processive runs on actin.
Topics: Actins; Adenosine Diphosphate; Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Biomechanical Phenomena; Deafness; Humans; Kinetics; Mice; Models, Biological; Models, Molecular; Mutant Proteins; Mutation; Myosin Heavy Chains; Protein Multimerization; Protein Structure, Tertiary; Sus scrofa; Urea | 2015 |
Ensemble force changes that result from human cardiac myosin mutations and a small-molecule effector.
Topics: Actin Cytoskeleton; Actins; Adenosine Triphosphatases; Animals; Biomechanical Phenomena; Cardiomyopathies; Cattle; Humans; Mice; Models, Biological; Models, Molecular; Mutation; Small Molecule Libraries; Software; Statistics as Topic; Urea; Utrophin; Ventricular Myosins | 2015 |
Myosin Activator Omecamtiv Mecarbil Increases Myocardial Oxygen Consumption and Impairs Cardiac Efficiency Mediated by Resting Myosin ATPase Activity.
Topics: Animals; Cardiotonic Agents; Disease Models, Animal; Dose-Response Relationship, Drug; Energy Metabolism; Enzyme Activation; Enzyme Activators; Female; Heart Failure; Male; Mice; Myocardial Contraction; Myocardial Infarction; Myocardium; Myosins; Oxygen Consumption; Stroke Volume; Sus scrofa; Urea; Ventricular Dysfunction, Left; Ventricular Function, Left | 2015 |
Omecamtiv Mecarbil, a Cardiac Myosin Activator, Increases Ca2+ Sensitivity in Myofilaments With a Dilated Cardiomyopathy Mutant Tropomyosin E54K.
Topics: Animals; Calcium; Cardiac Myosins; Cardiomyopathy, Dilated; Disease Models, Animal; Mice, Transgenic; Mutation; Myofibrils; Tropomyosin; Urea | 2015 |
Molecular effects of the myosin activator omecamtiv mecarbil on contractile properties of skinned myocardium lacking cardiac myosin binding protein-C.
Topics: Animals; Calcium; Carrier Proteins; Enzyme Activators; Female; Humans; Kinetics; Male; Mice, 129 Strain; Mice, Knockout; Myocardial Contraction; Myocardium; Myosins; Phosphorylation; Protein Processing, Post-Translational; Sarcomeres; Urea | 2015 |
Structural basis for drug-induced allosteric changes to human β-cardiac myosin motor activity.
Topics: Allosteric Regulation; Allosteric Site; Animals; Cardiac Myosins; Cell Line; Green Fluorescent Proteins; Humans; Mice; Protein Structure, Tertiary; Urea | 2015 |
A myosin activator improves actin assembly and sarcomere function of human-induced pluripotent stem cell-derived cardiomyocytes with a troponin T point mutation.
Topics: Actins; Animals; Animals, Newborn; Cardiac Myosins; Cardiotonic Agents; Cell Line; Dose-Response Relationship, Drug; Enzyme Activation; Enzyme Activators; Genotype; Humans; Induced Pluripotent Stem Cells; Myocardial Contraction; Myocytes, Cardiac; Phenotype; Point Mutation; Rats, Sprague-Dawley; Sarcomeres; Time Factors; Troponin T; Urea | 2016 |
Incorporating development of a patient-reported outcome instrument in a clinical drug development program: examples from a heart failure program.
Topics: Aged; Aged, 80 and over; Cardiac Myosins; Cardiovascular Agents; Clinical Trials as Topic; Dizziness; Dyspnea; Edema; Fatigue; Female; Focus Groups; Heart Failure; Humans; Male; Middle Aged; Patient Reported Outcome Measures; Qualitative Research; Quality of Life; Sleep Initiation and Maintenance Disorders; United States; United States Food and Drug Administration; Urea | 2016 |
Dose-dependent electrophysiological effects of the myosin activator omecamtiv mecarbil in canine ventricular cardiomyocytes.
Topics: Action Potentials; Animals; Dogs; Female; Heart Ventricles; Male; Myocytes, Cardiac; Myosins; Patch-Clamp Techniques; Urea | 2016 |
Heart failure: Phase II trial results of omecamtiv mecarbil.
Topics: Cardiotonic Agents; Clinical Trials, Phase II as Topic; Heart Failure, Systolic; Humans; Randomized Controlled Trials as Topic; Urea | 2017 |
Omecamtiv Mecarbil Enhances the Duty Ratio of Human β-Cardiac Myosin Resulting in Increased Calcium Sensitivity and Slowed Force Development in Cardiac Muscle.
Topics: Actins; Actomyosin; Adenosine Diphosphate; Animals; Calcium; Dose-Response Relationship, Drug; Humans; Kinetics; Mass Spectrometry; Mice; Myocardium; Myosins; Protein Domains; Recombinant Proteins; Stress, Mechanical; Urea; Ventricular Myosins | 2017 |
Heart failure drug changes the mechanoenzymology of the cardiac myosin powerstroke.
Topics: Animals; Biosensing Techniques; Cardiac Myosins; Cardiovascular Agents; Cattle; Chickens; Heart Failure; Humans; Kinetics; Myocardial Contraction; Myocardium; Myosins; Phosphates; Rabbits; Urea | 2017 |
Omecamtiv mecarbil activates ryanodine receptors from canine cardiac but not skeletal muscle.
Topics: Animals; Dogs; Dose-Response Relationship, Drug; Female; Heart; Male; Muscle, Skeletal; Myocardium; Rabbits; Ryanodine Receptor Calcium Release Channel; Urea | 2017 |
Mechanistic and structural basis for activation of cardiac myosin force production by omecamtiv mecarbil.
Topics: Animals; Binding Sites; Cardiac Myosins; Cattle; Crystallization; Protein Conformation; Urea | 2017 |
Omecamtiv Mecarbil Abolishes Length-Mediated Increase in Guinea Pig Cardiac Myofiber Ca
Topics: Animals; Biomechanical Phenomena; Calcium; Dose-Response Relationship, Drug; Guinea Pigs; Myocardial Contraction; Phosphorylation; Sarcomeres; Urea | 2017 |
Frequency-dependent effects of omecamtiv mecarbil on cell shortening of isolated canine ventricular cardiomyocytes.
Topics: Action Potentials; Animals; Calcium Signaling; Cell Size; Diastole; Dogs; Female; Heart Ventricles; Male; Myocardial Contraction; Myocytes, Cardiac; Myosins; Systole; Urea | 2017 |
Omecamtiv mercabil and blebbistatin modulate cardiac contractility by perturbing the regulatory state of the myosin filament.
Topics: Actin Cytoskeleton; Animals; Calcium; Cardiac Myosins; Heterocyclic Compounds, 4 or More Rings; Male; Myocardial Contraction; Myocardium; Myocytes, Cardiac; Rats; Rats, Wistar; Signal Transduction; Urea | 2018 |
Allosteric modulation of cardiac myosin dynamics by omecamtiv mecarbil.
Topics: Allosteric Regulation; Allosteric Site; Cardiac Myosins; Crystallography, X-Ray; Humans; Molecular Dynamics Simulation; Protein Conformation; Urea | 2017 |
Effects of the cardiac myosin activator Omecamtiv-mecarbil on severe chronic aortic regurgitation in Wistar rats.
Topics: Animals; Aortic Valve; Aortic Valve Insufficiency; Cardiac Myosins; Cardiovascular Agents; Chronic Disease; Disease Models, Animal; Echocardiography, Doppler; Hemodynamics; Infusions, Intravenous; Male; Rats, Wistar; Recovery of Function; Severity of Illness Index; Stroke Volume; Urea; Ventricular Function, Left | 2018 |
Perspectives of a myosin motor activator agent with increased selectivity.
Topics: Animals; Cardiac Myosins; Clinical Trials, Phase III as Topic; Computer Simulation; Dogs; Heart Failure; Humans; Molecular Docking Simulation; Myosin Heavy Chains; Protein Structure, Tertiary; Ryanodine Receptor Calcium Release Channel; Software; Structure-Activity Relationship; Urea | 2018 |
Controlling load-dependent kinetics of β-cardiac myosin at the single-molecule level.
Topics: Actins; Animals; Cattle; Dose-Response Relationship, Drug; Heart Ventricles; Humans; Kinetics; Mutation; Myocardial Contraction; Urea; Ventricular Myosins | 2018 |
Positive cardiac inotrope omecamtiv mecarbil activates muscle despite suppressing the myosin working stroke.
Topics: Adenosine Triphosphate; Animals; Cardiotonic Agents; Cell Line; Drug Evaluation, Preclinical; Mice; Monte Carlo Method; Myosins; Optical Tweezers; Swine; Urea | 2018 |
Treatments targeting inotropy.
Topics: Acute Disease; Animals; Antioxidants; Calcium; Cardiotonic Agents; Case-Control Studies; Catecholamines; Clinical Trials as Topic; Diastole; Dobutamine; Dogs; Energy Metabolism; Excitation Contraction Coupling; Heart Failure; Humans; Mitochondria; Models, Animal; Myocardial Contraction; Nitrogen Oxides; Oxidation-Reduction; Phosphodiesterase Inhibitors; Placebos; Receptors, Adrenergic; Sarcomeres; Shock, Cardiogenic; Simendan; Swine; Systole; Urea | 2019 |
Opposite diastolic effects of omecamtiv mecarbil versus dobutamine and ivabradine co-treatment in pigs with acute ischemic heart failure.
Topics: Animals; Cardiotonic Agents; Cardiovascular Agents; Diastole; Dobutamine; Drug Therapy, Combination; Heart Failure; Ivabradine; Male; Myocardial Ischemia; Swine; Treatment Outcome; Urea | 2018 |
SarcTrack.
Topics: Algorithms; Benzylamines; Cardiovascular Agents; Carrier Proteins; Clustered Regularly Interspaced Short Palindromic Repeats; Computer-Aided Design; Fluorescence; Humans; Induced Pluripotent Stem Cells; Microscopy, Atomic Force; Myocardial Contraction; Myocytes, Cardiac; Myosins; Propranolol; Sarcomeres; Software; Uracil; Urea; Verapamil; Video Recording | 2019 |
Omecamtiv Mecarbil Slows Myosin Kinetics in Skinned Rat Myocardium at Physiological Temperature.
Topics: Animals; Calcium; Kinetics; Male; Myocardium; Myosins; Rats; Rats, Sprague-Dawley; Temperature; Urea | 2019 |
Dilated cardiomyopathy mutation in the converter domain of human cardiac myosin alters motor activity and response to omecamtiv mecarbil.
Topics: Actin Cytoskeleton; Actins; Actomyosin; Adenosine Triphosphatases; Cardiomyopathy, Dilated; Heart Failure; Humans; Kinetics; Motor Activity; Mutation; Myocardial Contraction; Protein Domains; Urea; Ventricular Myosins | 2019 |
Combined Therapy With Dobutamine and Omecamtiv Mecarbil in Pigs With Ischemic Acute Heart Failure Is Attributed to the Effect of Dobutamine.
Topics: Acute Disease; Animals; Cardiac Output; Cardiotonic Agents; Disease Models, Animal; Dobutamine; Drug Therapy, Combination; Energy Metabolism; Heart Failure; Male; Myocardial Contraction; Myocardial Ischemia; Oxygen Consumption; Sus scrofa; Urea; Ventricular Function, Left | 2020 |
Targeted and Controlled Drug Delivery to a Rat Model of Heart Failure Through a Magnetic Nanocomposite.
Topics: Animals; Cell Line; Disease Models, Animal; Drug Delivery Systems; Heart Failure; Magnetic Fields; Male; Myocardium; Nanocomposites; Rats; Rats, Wistar; Urea | 2020 |
Omecamtiv mecarbil lowers the contractile deficit in a mouse model of nebulin-based nemaline myopathy.
Topics: Animals; Calcium; Disease Models, Animal; Mice; Mice, Knockout; Muscle Contraction; Muscle Fibers, Skeletal; Muscle Proteins; Myopathies, Nemaline; Urea | 2019 |
Optimizing heart failure management: anticoagulation, diuretic withdrawal, iron substitution, and novel inotropes.
Topics: Acute Disease; Anemia, Iron-Deficiency; Anticoagulants; Cardiotonic Agents; Case-Control Studies; Diuretics; Factor Xa Inhibitors; Heart Aneurysm; Heart Failure; Humans; Hypertension; Iron; Myocardial Infarction; Pacemaker, Artificial; Percutaneous Coronary Intervention; Placebos; Portraits as Topic; Rivaroxaban; Stroke; Stroke Volume; Thrombosis; Urea | 2019 |
Force and Calcium Transients Analysis in Human Engineered Heart Tissues Reveals Positive Force-Frequency Relation at Physiological Frequency.
Topics: Artifacts; Biomechanical Phenomena; Calcium Signaling; Fluorescence; Heart; Humans; Motion; Myocardial Contraction; Tissue Engineering; Urea | 2020 |
Myosin from the ventricle is more sensitive to omecamtiv mecarbil than myosin from the atrium.
Topics: Actins; Animals; Heart Atria; Heart Ventricles; Myocardial Contraction; Myosins; Protein Interaction Maps; Swine; Urea | 2020 |
The Galaxy of Cytoskeletal Modulation in the Universe of Heart Failure Therapeutics.
Topics: Chronic Disease; Heart Failure; Humans; Urea | 2020 |
Orthophosphate increases the efficiency of slow muscle-myosin isoform in the presence of omecamtiv mecarbil.
Topics: Adenosine Triphosphatases; Animals; Calcium; Cardiac Myosins; Drug Synergism; Male; Muscle, Skeletal; Myocardial Contraction; Myosins; Phosphates; Rabbits; Sarcomeres; Stress, Mechanical; Urea | 2020 |
Single-Cell Mechanical Analysis of Human Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Testing and Pathophysiological Studies.
Topics: Biomechanical Phenomena; Cell Differentiation; Cell Line; Cell Shape; Doxorubicin; Drug Evaluation, Preclinical; Humans; Myocardial Contraction; Myocytes, Cardiac; Pluripotent Stem Cells; Single-Cell Analysis; Urea | 2020 |
Effects of omecamtiv mecarbil on calcium-transients and contractility in a translational canine myocyte model.
Topics: Animals; Calcium Signaling; Dogs; Dose-Response Relationship, Drug; Fura-2; Heart Ventricles; Humans; Isoproterenol; Male; Models, Animal; Muscle Cells; Muscle Contraction; Sarcomeres; Urea | 2020 |
Stimulation of Contractility in Systolic Heart Failure.
Topics: Heart Failure; Heart Failure, Systolic; Humans; Urea | 2021 |
Truly galactic?
Topics: Cardiac Myosins; Heart Failure, Systolic; Humans; Urea | 2021 |
Heart failure or heart success?
Topics: Cardiovascular Agents; Evidence-Based Medicine; Ferric Compounds; Glycosides; Heart Failure, Systolic; Hospitalization; Humans; Maltose; Randomized Controlled Trials as Topic; Recovery of Function; Research Design; Sodium-Glucose Transporter 1; Sodium-Glucose Transporter 2 Inhibitors; Stroke Volume; Treatment Outcome; Urea; Ventricular Function, Left | 2021 |
Myosin with hypertrophic cardiac mutation R712L has a decreased working stroke which is rescued by omecamtiv mecarbil.
Topics: Cardiomegaly; Cardiotonic Agents; Heart Failure; Humans; Mutation; Urea; Ventricular Myosins | 2021 |
cMyBPC phosphorylation modulates the effect of omecamtiv mecarbil on myocardial force generation.
Topics: Animals; Humans; Mice; Myocardial Contraction; Myocardium; Phosphorylation; Urea | 2021 |
Omecamtiv Mecarbil use in systolic heart failure- Results of the GALACTIC-HF trial.
Topics: Cardiotonic Agents; Heart Failure, Systolic; Humans; Randomized Controlled Trials as Topic; Urea | 2021 |
The effect of the cardiac myosin activator, omecamtiv mecarbil, on right ventricular structure and function in chronic systolic heart failure (COSMIC-HF).
Topics: Cardiac Myosins; Heart Failure; Heart Failure, Systolic; Humans; Stroke Volume; Urea | 2021 |
New saviour for an old problem: Omecamtiv mecarbil for systolic heart failure.
Topics: Heart Failure; Heart Failure, Systolic; Humans; Urea | 2021 |
Effects of omecamtiv mecarbil on failing human ventricular trabeculae and interaction with (-)-noradrenaline.
Topics: Adrenergic alpha-Agonists; Adult; Aged; Female; Heart Failure; Heart Ventricles; Humans; Male; Middle Aged; Myocardial Contraction; Norepinephrine; Urea; Ventricular Function | 2021 |
Comprehensive in vitro pro-arrhythmic assays demonstrate that omecamtiv mecarbil has low pro-arrhythmic risk.
Topics: Action Potentials; Animals; Arrhythmias, Cardiac; Computer Simulation; Dogs; Drug Evaluation, Preclinical; Heart Failure; Heart Ventricles; Humans; Isolated Heart Preparation; Myocytes, Cardiac; Primary Cell Culture; Purkinje Fibers; Rabbits; Urea | 2021 |
Evidence for synergy between sarcomeres and fibroblasts in an in vitro model of myocardial reverse remodeling.
Topics: Actomyosin; Animals; Animals, Newborn; Benzamides; Benzylamines; Cardiac Myosins; Cell Line; Dioxoles; Heart Failure; Humans; Induced Pluripotent Stem Cells; Myocardial Contraction; Myocardium; Myocytes, Cardiac; Myofibroblasts; Rats; Rats, Sprague-Dawley; Receptor, Transforming Growth Factor-beta Type I; Sarcomeres; Signal Transduction; Swine; Tissue Engineering; Tissue Scaffolds; Uracil; Urea; Ventricular Remodeling | 2021 |
Omecamtiv Mecarbil in Systolic Heart Failure.
Topics: Cardiac Myosins; Heart Failure, Systolic; Humans; Stroke Volume; Urea | 2021 |
Omecamtiv Mecarbil in Systolic Heart Failure.
Topics: Cardiac Myosins; Heart Failure, Systolic; Humans; Stroke Volume; Urea | 2021 |
Omecamtiv Mecarbil in Systolic Heart Failure.
Topics: Cardiac Myosins; Heart Failure, Systolic; Humans; Stroke Volume; Urea | 2021 |
Omecamtiv Mecarbil in Systolic Heart Failure. Reply.
Topics: Heart Failure, Systolic; Humans; Stroke Volume; Urea | 2021 |
Omecamtiv Mecarbil: A Personalized Treatment for Patients With Severely Impaired Ejection Fraction.
Topics: Humans; Precision Medicine; Stroke Volume; Urea; Ventricular Function, Left | 2021 |
Danicamtiv Enhances Systolic Function and Frank-Starling Behavior at Minimal Diastolic Cost in Engineered Human Myocardium.
Topics: Animals; Cardiotonic Agents; Cell Line; Humans; Induced Pluripotent Stem Cells; Kinetics; Male; Middle Aged; Models, Cardiovascular; Myocardial Contraction; Myocytes, Cardiac; Sus scrofa; Systole; Tissue Engineering; Tissue Scaffolds; Urea | 2021 |
Effect of Omecamtiv Mecarbil on the Pharmacokinetics of Metformin, a Probe Substrate for MATE1/MATE2-K, in Healthy Subjects.
Topics: Administration, Oral; Adult; Area Under Curve; Diarrhea; Drug Interactions; Female; Half-Life; Healthy Volunteers; Humans; Least-Squares Analysis; Male; Metformin; Middle Aged; Organic Cation Transport Proteins; ROC Curve; Substrate Specificity; Tablets; Urea | 2021 |
Effect of Varying Degrees of Hepatic Impairment on the Pharmacokinetics of Omecamtiv Mecarbil.
Topics: Administration, Oral; Area Under Curve; Humans; Tablets; Urea | 2021 |
Pharmacokinetic Evaluation of the CYP3A4 and CYP2D6 Drug-Drug Interaction and CYP3A4 Induction Potential of Omecamtiv Mecarbil: Two Open-Label Studies in Healthy Subjects.
Topics: Cytochrome P-450 CYP2D6; Cytochrome P-450 CYP3A; Drug Interactions; Healthy Volunteers; Humans; Urea | 2022 |
Pharmacokinetic Drug-Drug Interaction Study of Omecamtiv Mecarbil With Omeprazole, a Proton Pump Inhibitor, in Healthy Subjects.
Topics: Drug Interactions; Healthy Volunteers; Humans; Omeprazole; Proton Pump Inhibitors; Urea | 2022 |
The myosin activator omecamtiv mecarbil improves wall stress in a rat model of chronic aortic regurgitation.
Topics: Animals; Aortic Valve Insufficiency; Cardiotonic Agents; Heart Ventricles; Infusions, Intravenous; Male; Rats; Rats, Wistar; Stroke Volume; Systole; Urea | 2021 |
Evaluation of drug-drug interaction potential between omecamtiv mecarbil and rosuvastatin, a BCRP substrate, with a clinical study in healthy subjects and using a physiologically-based pharmacokinetic model.
Topics: Adult; ATP Binding Cassette Transporter, Subfamily G, Member 2; Biomedical Research; Drug Interactions; Female; Healthy Volunteers; Humans; Male; Models, Biological; Neoplasm Proteins; Rosuvastatin Calcium; Urea | 2021 |
[CLINICAL EFFICACY OF A REPRESENTATIVE OF A NEW CLASS OF INOTROPIC AGENTS - THE DIRECT ACTIVATOR OF MYOSIN OF CARDIOMYOCYTES OMECAMTIV MECARBIL IN HEART FAILURE WITH A REDUCED EJECTION FRACTION].
Topics: Heart Failure; Humans; Myocytes, Cardiac; Myosins; Quality of Life; Stroke Volume; Treatment Outcome; Urea | 2021 |
Pharmacokinetic Drug-Drug Interaction Study of Omecamtiv Mecarbil With Amiodarone and Digoxin in Healthy Subjects.
Topics: Amiodarone; Clinical Trials, Phase I as Topic; Digoxin; Drug Interactions; Healthy Volunteers; Humans; Urea | 2022 |
Generative adversarial networks for construction of virtual populations of mechanistic models: simulations to study Omecamtiv Mecarbil action.
Topics: Animals; Myocardial Contraction; Myocytes, Cardiac; Myosins; Rats; Urea | 2022 |
Population Pharmacokinetic Properties of Omecamtiv Mecarbil in Healthy Subjects and Patients With Heart Failure With Reduced Ejection Fraction.
Topics: Healthy Volunteers; Heart Failure; Humans; Stroke Volume; Urea | 2022 |
Comprehensive analyses of the inotropic compound omecamtiv mecarbil in rat and human cardiac preparations.
Topics: Adenosine Triphosphate; Animals; Calcium; Cardiotonic Agents; Cell Line; Cells, Cultured; Cellular Reprogramming Techniques; Humans; Induced Pluripotent Stem Cells; Mitochondria, Heart; Myocardial Contraction; Myocytes, Cardiac; Rats; Rats, Wistar; Reactive Oxygen Species; Urea | 2022 |
Omecamtiv mecarbil treatment improves post-resuscitation cardiac function and neurological outcome in a rat model.
Topics: Animals; Cardiopulmonary Resuscitation; Heart Arrest; Male; Myocardial Contraction; Nervous System Diseases; Rats; Rats, Wistar; Stroke Volume; Urea; Ventricular Dysfunction; Ventricular Function, Left | 2022 |
A deleterious interaction between omecamtiv mecarbil and atrial fibrillation in patients with heart failure: an influence of digoxin?
Topics: Atrial Fibrillation; Digoxin; Heart Failure; Humans; Urea | 2022 |
Omecamtiv Mecarbil as a Therapy for Heart Failure With Low Ejection Fraction.
Topics: Heart Failure; Humans; Stroke Volume; Urea; Ventricular Function, Left | 2022 |
Omecamtiv mecarbil for patients with severe systolic dysfunction and hypotension.
Topics: Blood Pressure; Heart Failure; Humans; Hypotension; Stroke Volume; Urea; Ventricular Dysfunction, Left | 2022 |
Omecamtiv Mecarbil: Decisional Dilemmas and Regulatory Science - Opportunities for Improvement?
Topics: Heart Failure; Humans; Myocardial Contraction; Stroke Volume; Urea | 2023 |
Potential Applicability of Omecamtiv Mecarbil to Patients Hospitalized for Worsening Heart Failure.
Topics: Heart Failure; Humans; Urea | 2023 |