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MRTX849

The Clinical Trial to Evaluate the Pharmacokinetics and Safety of MRTX849 in Patients With Advanced Solid Tumors

Ensayo de Zai Lab Ltd en Advanced or Metastatic Solid Tumor (del registro, en inglés).

Fase

Fase 1

Estado

Sin noticias del promotor

Participantes

22

previstos

Centros

8

Fin del objetivo primario

oct 2023

estimado por el promotor

Qué significa cada fase y cada estado.

Estudio de intervención, de un solo grupo, abierto. Comenzó en may 2022.

Qué mide

Main PK parameters: Cmax (Approximately 2 weeks after dose initiation) (del registro, en inglés)

Cómo lo describe el promotor

En el documentoEn inglés, del registroThis is a phase 1, open-label, single-arm study in Chinese patients with unresectable, locally advanced or metastatic solid tumor with KRAS G12C mutation, for which treatment with curative intent is not available. Patients must have a documented KRAS G12C mutation determined by tissue or liquid-based local testing. The PK profile of MRTX849 in Chinese patients will be evaluated after administration of a single and repeat oral doses of 600 mg BID. In the PK lead-in period, blood samples will be collected pre-dose and up to 96 hours post a single oral dose of 600 mg MRTX849. Following this lead-in period, patients will start the dosing regimen of 600 mg BID orally, and blood samples will be collected pre-dose and up to 12 hours after multiple doses of MRTX849 600 mg BID on Cycle 1 Day 8 (C1D8). Safety including AEs, ECGs, laboratory parameters and vital signs of each patient will be monitored throughout the conduct of the study. Disease response and progression will be evaluated in accordance with Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1).

Más ensayos de ZLAB

Todos los de ZLAB, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT05263986), actualizada en feb 2023.