A Phase 1 First-In-Human Study of the Anti-CD73 IPH5301 Alone or in Combination With Chemotherapy and Trastuzumab in Patients With Advanced Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

January 21, 2022

Primary Completion Date

March 31, 2025

Study Completion Date

February 28, 2026

Conditions
Metastatic CancerMetastatic Breast CancerMetastatic Pancreatic CancerMetastatic Gastric CancerMetastatic Lung CancerMetastatic Ovary CancerOesophageal CancerEndometrial CancerAdvanced Solid Tumor
Interventions
DRUG

IPH5301 ALONE OR IN COMBINATION WITH CHEMOTHERAPY AND TRASTUZUMAB

"Part I-Dose escalation Patients will receive IPH5301 alone on day 1 (Week 1). Treatment will be administered every 2 weeks until progression or unacceptable toxicity or other reasons requiring treatment discon-tinuation, for a maximum duration of 12 months.~Part II- Expansion cohort Patients will receive IPH5301 at a recommended dose (RP2D) or a next lower dose (RP2D-1)in combination with trastuzumab and paclitaxel, at day 1 and every 2 weeks up to 6 cycles of paclitaxel. The RP2D dose will not exceed the designated maximum tolerated dose (MTD)."

Trial Locations (1)

Unknown

RECRUITING

Institut Paoli Calmettes, Marseille

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Innate Pharma

INDUSTRY

lead

Institut Paoli-Calmettes

OTHER

NCT05143970 - A Phase 1 First-In-Human Study of the Anti-CD73 IPH5301 Alone or in Combination With Chemotherapy and Trastuzumab in Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter