Safety, Pharmacokinetics and Preliminary Efficacy of CS231295 in Advanced Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

102

Participants

Timeline

Start Date

May 21, 2025

Primary Completion Date

April 30, 2029

Study Completion Date

April 30, 2029

Conditions
NeoplasmsGlioblastoma, AdultSmall Cell Lung Carcinoma (SCLC)
Interventions
DRUG

CS231295

oral tablet. Only one dose on C0D1 in single-dose period. Once daily from C1D1 until disease progression, death, intolerable toxicity, loss to follow-up, withdrawal of informed consent, or the end of the trial, whichever occurs first, in multiple-dose period in both escalation and cohort expansion phases.

Trial Locations (2)

100070

NOT_YET_RECRUITING

Beijing Tiantan Hospital, Capital Medical University, Beijing

130103

RECRUITING

Jilin Cancer Hospital, Changchun

Sponsors
All Listed Sponsors
lead

Chipscreen Biosciences, Ltd.

INDUSTRY