Page last updated: 2024-10-15

sc002

Description

SC002: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID131954443
MeSH IDM0393124

Synonyms (13)

Synonym
sc-002
rovalpituzumab-tesirin
rovalpituzumab tesirine
rovalpituzumab tesirine [usan:inn:who-dd]
1613313-09-9
sc002
sc0002
rovalpituzumab tesirine [inn]
rovalpituzumab tesirine [usan:inn]
rovalpituzumab tesirine [who-dd]
unii-p256hb60ff
rova-t
p256hb60ff ,

Toxicity

ExcerptReference
" The most common treatment-related adverse events (≥25% of patients, all grades) were platelet count decreased, pleural effusion, peripheral edema, aspartate aminotransferase increased, white blood cell count decreased, neutrophil count decreased, alanine aminotransferase increased, hypoalbuminaemia, anemia and decreased appetite."( Phase I safety and pharmacokinetics study of rovalpituzumab tesirine in Japanese patients with advanced, recurrent small cell lung cancer.
Akamatsu, H; Fujiwara, Y; Kanda, S; Kirita, K; Kosloski, MP; Nakagawa, K; Okamoto, I; Okubo, S; Scripture, C; Shintani, M; Takeda, M; Tamura, T; Tanaka, K; Teraoka, S; Udagawa, H; Yasuda, I, 2019
)
" The most common adverse events (AE) were fatigue, photosensitivity reaction, and pleural effusion."( Efficacy and Safety of Rovalpituzumab Tesirine in Third-Line and Beyond Patients with DLL3-Expressing, Relapsed/Refractory Small-Cell Lung Cancer: Results From the Phase II TRINITY Study.
Besse, B; Carbone, DP; Dowlati, A; Farago, AF; Glisson, BS; Govindan, R; Greillier, L; Hann, CL; Lally, S; Le Moulec, S; Morgensztern, D; Ready, N; Rudin, CM; Santana-Davila, R; Wolf, J; Yalamanchili, S, 2019
)
" The combination was tolerated, with the most common treatment-emergent adverse events (in >30%) being pleural effusion, fatigue, and cough."( Safety, pharmacokinetics, and efficacy of budigalimab with rovalpituzumab tesirine in patients with small cell lung cancer.
Afar, DE; Alanko, T; Calvo, E; Cassier, PA; Englert, S; Gao, B; Gazzah, A; Italiano, A; Komarnitsky, P; Kondo, S; Lambert, S; Miguel, M; Millward, M; Moreno, V; Parikh, A; Peltola, K; Prenen, H; Rottey, S; Seto, T; Spira, A; Toyozawa, R; Vosganian, G; Warburton, L; Yoh, K, 2021
)

Dosage Studied

ExcerptReference
" Cohort 2 received the same dosage of Rova-T as cohort 1 plus 1 mg/kg nivolumab (four 3-wk cycles) and 1 mg/kg ipilimumab (beginning week 4)."( A Phase 1-2 Study of Rovalpituzumab Tesirine in Combination With Nivolumab Plus or Minus Ipilimumab in Patients With Previously Treated Extensive-Stage SCLC.
Besse, B; Blot, V; Curigliano, G; Greillier, L; Johnson, ML; Lally, S; Leal, T; Lehman, J; Maag, D; Malhotra, J; Morgensztern, D; Nikolinakos, P; Patel, JD; Ready, N; Robinet, G; Valenzuela, R; Wrangle, JM, 2021
)
"A total of 26 patients were dosed (cohort 3: 14; cohorts 1, 2, and 4 combined: 12)."( A Phase 1 Study Evaluating Rovalpituzumab Tesirine in Frontline Treatment of Patients With Extensive-Stage SCLC.
Burns, TF; Camidge, DR; Chen, C; Dowlati, A; Hann, CL; Koch, MM; Komarnitsky, P; Ludwig, C; Morgensztern, D; Nimeiri, H; Patel, M; Ward, PJ, 2021
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (30)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's17 (56.67)24.3611
2020's13 (43.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials10 (32.26%)5.53%
Reviews8 (25.81%)6.00%
Case Studies2 (6.45%)4.05%
Observational0 (0.00%)0.25%
Other11 (35.48%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]