Ph Ib RMC-6291 in Comb w/ RMC-6236 in Pts w/ Adv KRASG12C Mutated Solid Tumors

Cancer
Sai-Hong Ou
Phase 1b, Multicenter, Open-Label, Dose Escalation and Dose Expansion Study of RMC-6291 in Combination with RMC-6236 in Participants with Advanced KRAS G12C-Mutated Solid Tumors
Anus
Bones and Joints
Brain and Nervous System
Breast
Cervix
Colon
Corpus Uteri
Esophagus
Eye and Orbit
Ill-Defined Sites
Kaposis sarcoma
Kidney
Larynx
Lip Oral Cavity and Pharynx
Liver
Lung
Melanoma skin
Other Digestive Organ
Other Endocrine System
Other Female Genital
Other Male Genital
Other Respiratory and Intrathoracic Organs
Other Skin
Other Urinary
Ovary
Pancreas
Prostate
Rectum
Small Intestine
Soft Tissue
Stomach
Thyroid
Unknown Sites
Urinary Bladder

Study Description

This study is to evaluate the safety, tolerability, and PK profiles of RMC-6291 and RMC-6236 in adults with KRAS G12C-mutated solid tumors.

Eligibility

18 years of age

Histology: pathologically, KRAS G12C-mutated, documented advanced or metastatic solid tumors not amendable to curative therapy

Part 1. Dose Escalation: solid tumors, previously treated

Part 2. Dose Expansion:

i.Non-small cell lung cancer (NSCLC), previously treated with immunotherapy, chemotherapy, and KRAS G12C (OFF) inhibitors,

ii. NSCLC, previously treated with immunotherapy and chemotherapy, naïve to KRAS G12C (OFF) inhibitors,

iii. NSCLC, previously treated with immunotherapy, chemotherapy, with untreated, asymptomatic central nervous system (CNS) metastases <2 cm in size

iv. Solid tumors, previously treated, naïve to KRAS G12C (OFF) inhibitors.

ECOG performance status 0 or 1

Adequate organ function

i. Primary central nervous system (CNS) tumors

ii. Active brain metastases

iii. Known impairment of gastrointestinal function that would alter the absorption

iv. Major surgical procedures within 28 days or non-study related minor procedures within 7 days of treatment

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