A Phase 2 Study of HX301 in Patients with High-grade Giloma

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

January 8, 2025

Primary Completion Date

December 31, 2026

Study Completion Date

December 31, 2028

Conditions
Glioma
Interventions
DRUG

HX301+/Temozolomide

"Part I: It is planned to firstly explore a dose of 160 mg and enroll approximately 3-6 subjects to receive HX301 monotherapy until disease progression, intolerable toxicity, or other reasons for stopping treatment for up to 24 cycles of 28 days each. Safety evaluation was performed using the traditional 3 + 3 rule, and the DLT observation period was 28 days (C1D1 \~ C1D28). If 160 mg was not tolerated, it was reduced to 120 mg for exploration. Part II: Combination therapy phase: HX301 will be administered in combination with temozolomide approximately 4-6 weeks after completion of chemoradiotherapy. The TMZ dose will follow the first cycle: 150 mg/m 2 qd D1-D5, starting with the second cycle, and if the criteria for TMZ dose increase are met, TMZ will be administered as 200 mg/m 2 qd D1-D5 every 2 8 days for up to 12 cycles. Monotherapy maintain period: Following the end of temozolomide treatment, HX301 monotherapy will be continued for a maximum of 12 cycles of 28 days each."

Trial Locations (1)

100083

RECRUITING

Beijing Tiantan Hospital Capital Medical University, Beijing

All Listed Sponsors
lead

Hangzhou Hanx Biopharmaceuticals, Ltd.

INDUSTRY

NCT06703255 - A Phase 2 Study of HX301 in Patients with High-grade Giloma | Biotech Hunter | Biotech Hunter