hexamethylene bisacetamide has been researched along with Thrombopenia in 4 studies
N,N'-diacetyl-1,6-diaminohexane: chemical name obtained from Acta Biol Hung 1990;41(1-3):199-208
Excerpt | Relevance | Reference |
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"Hexamethylene bisacetamide (HMBA) is a potent inducer of differentiation of a number of transformed cell lines in vitro." | 6.67 | Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia: a phase II clinical trial with a differentiation-inducing agent. ( Andreeff, M; Ervin, T; Kufe, D; Marks, PA; Michaeli, J; Rifkind, RA; Sogoloff, H; Stone, R; Tong, WP; Young, CW, 1992) |
"The efficacy of hexamethylene bisacetamide (HMBA), a potent polar-planar solvent which is capable of differentiating leukemias and solid tumors in vitro at clinically achievable concentrations, was studied in 16 patients with severe myelodysplastic syndromes (MDS)." | 3.68 | Hexamethylene bisacetamide in myelodysplastic syndrome: effect of five-day exposure to maximal therapeutic concentrations. ( Auerbach, M; Conley, BA; Donehower, RC; Jones, RJ; Rowinsky, EK; Spivak, JL, 1992) |
"Hexamethylene bisacetamide (HMBA) is a potent inducer of differentiation of a number of transformed cell lines in vitro." | 2.67 | Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia: a phase II clinical trial with a differentiation-inducing agent. ( Andreeff, M; Ervin, T; Kufe, D; Marks, PA; Michaeli, J; Rifkind, RA; Sogoloff, H; Stone, R; Tong, WP; Young, CW, 1992) |
"Hexamethylene bisacetamide was administered as a 5% (w/v) solution via a nasogastric or gastrostomy tube every 4 h for 5 days, followed in 21 days by a 5-day continuous i." | 2.67 | Phase I bioavailability and pharmacokinetic study of hexamethylene bisacetamide (NSC 95580) administered via nasogastric tube. ( Chun, HG; Kelley, JA; Leyland-Jones, B; Lombardo, FA; Roth, JS; Ward, FT; Weiss, RB, 1991) |
"6 g/m2/day), we attempted to individualize each patient's dose based on a dosing scheme using an adaptive (feedback) control algorithm, which assumed linear clearance for HMBA." | 1.28 | Phase I trial using adaptive control dosing of hexamethylene bisacetamide (NSC 95580). ( Conley, BA; Egorin, MJ; Forrest, A; Sinibaldi, V; Van Echo, DA; Zuhowski, EG, 1989) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 3 (75.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andreeff, M | 1 |
Stone, R | 1 |
Michaeli, J | 1 |
Young, CW | 1 |
Tong, WP | 1 |
Sogoloff, H | 1 |
Ervin, T | 1 |
Kufe, D | 1 |
Rifkind, RA | 1 |
Marks, PA | 1 |
Rowinsky, EK | 1 |
Conley, BA | 2 |
Jones, RJ | 1 |
Spivak, JL | 1 |
Auerbach, M | 1 |
Donehower, RC | 1 |
Ward, FT | 1 |
Kelley, JA | 1 |
Roth, JS | 1 |
Lombardo, FA | 1 |
Weiss, RB | 1 |
Leyland-Jones, B | 1 |
Chun, HG | 1 |
Forrest, A | 1 |
Egorin, MJ | 1 |
Zuhowski, EG | 1 |
Sinibaldi, V | 1 |
Van Echo, DA | 1 |
2 trials available for hexamethylene bisacetamide and Thrombopenia
Article | Year |
---|---|
Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia: a phase II clinical trial with a differentiation-inducing agent.
Topics: Acetamides; Adolescent; Adult; Aged; Bone Marrow; Cell Differentiation; Hematopoietic Stem Cells; Hu | 1992 |
Phase I bioavailability and pharmacokinetic study of hexamethylene bisacetamide (NSC 95580) administered via nasogastric tube.
Topics: Acetamides; Adult; Aged; Biological Availability; Confusion; Drug Evaluation; Female; Gastrointestin | 1991 |
2 other studies available for hexamethylene bisacetamide and Thrombopenia
Article | Year |
---|---|
Hexamethylene bisacetamide in myelodysplastic syndrome: effect of five-day exposure to maximal therapeutic concentrations.
Topics: Acetamides; Adult; Aged; Algorithms; Cell Division; Depression, Chemical; Drug Administration Schedu | 1992 |
Phase I trial using adaptive control dosing of hexamethylene bisacetamide (NSC 95580).
Topics: Acetamides; Algorithms; Antineoplastic Agents; Drug Evaluation; Humans; Neoplasms; Thrombocytopenia | 1989 |