TriN 2755 is an alkylating antineoplastic agent for intravenous (IV) use, carrying the triazene group as the cytotoxic principal. Using a standard 3 + 3 design, a phase I study was performed in tumour bearing dogs to determine the maximum tolerated dose (MTD), the dose limiting toxicity (DLT), and pharmacokinetic (PK) profile of TriN 2755. Thirty dogs were included in the study. TriN 2755 was administered over 20 min on two consecutive weeks per month for a total of three cycles. The starting dose was 25 mg kg-1 and the MTD was 74.6 mg kg-1 . Three dogs experienced DLT, which was characterized by gastrointestinal adverse events. The PKs of TriN 2755 and its main metabolites in plasma and sputum are described in a two-compartment model. The ...
Background: A broad range of gemcitabine dosages have been used in dogs. Hypothesis/Objectives: To d...
Abstract Background Chemotherapeutic options for the treatment of canine lymphoma have not changed i...
To extend initial results on the antineoplastic activity of α-1,3,5-triglycidyl-s-triazinetrione (TG...
TriN 2755 is an alkylating antineoplastic agent for intravenous (IV) use which carries the triazene ...
Temozolomide is a novel oral alkylating agent that has schedule-dependent clinical activity in human...
The novel water soluble compound STA-1474 is metabolized to ganetespib (formerly STA-9090), a potent...
Housuoi.nnn, GLENN E. AND Ti Li Loo: Disposition of 5-(3,3-dimethyl-1-triazeno)imi-dazole-4-carboxam...
Development of iniparib as an anti-cancer agent was hindered in part by lingering questions regardin...
and inhibit tumor growth in the setting of murine xenografts. The purpose of the following study wa...
Introduction. Gemcitabine is a nucleoside analogue with unique metabolic and mechanistic properties....
Activation of one or both the Ras/MAPK and PI3K/Akt/mTOR signal transduction pathways are known to m...
BACKGROUND: A broad range of gemcitabine dosages have been used in dogs. HYPOTHESIS/OBJECTIVES: To...
Combretastatin A4-Phosphate (CA4P) is a vascular disrupting agent revealing promising results in can...
The objective of these studies was to evaluate the potential toxi-city of Triapine (a ribonucleotide...
<p>Combretastatin A4-Phosphate (CA4P) is a vascular disrupting agent revealing promising resul...
Background: A broad range of gemcitabine dosages have been used in dogs. Hypothesis/Objectives: To d...
Abstract Background Chemotherapeutic options for the treatment of canine lymphoma have not changed i...
To extend initial results on the antineoplastic activity of α-1,3,5-triglycidyl-s-triazinetrione (TG...
TriN 2755 is an alkylating antineoplastic agent for intravenous (IV) use which carries the triazene ...
Temozolomide is a novel oral alkylating agent that has schedule-dependent clinical activity in human...
The novel water soluble compound STA-1474 is metabolized to ganetespib (formerly STA-9090), a potent...
Housuoi.nnn, GLENN E. AND Ti Li Loo: Disposition of 5-(3,3-dimethyl-1-triazeno)imi-dazole-4-carboxam...
Development of iniparib as an anti-cancer agent was hindered in part by lingering questions regardin...
and inhibit tumor growth in the setting of murine xenografts. The purpose of the following study wa...
Introduction. Gemcitabine is a nucleoside analogue with unique metabolic and mechanistic properties....
Activation of one or both the Ras/MAPK and PI3K/Akt/mTOR signal transduction pathways are known to m...
BACKGROUND: A broad range of gemcitabine dosages have been used in dogs. HYPOTHESIS/OBJECTIVES: To...
Combretastatin A4-Phosphate (CA4P) is a vascular disrupting agent revealing promising results in can...
The objective of these studies was to evaluate the potential toxi-city of Triapine (a ribonucleotide...
<p>Combretastatin A4-Phosphate (CA4P) is a vascular disrupting agent revealing promising resul...
Background: A broad range of gemcitabine dosages have been used in dogs. Hypothesis/Objectives: To d...
Abstract Background Chemotherapeutic options for the treatment of canine lymphoma have not changed i...
To extend initial results on the antineoplastic activity of α-1,3,5-triglycidyl-s-triazinetrione (TG...