A Trial of SHR-A2102 With Other Antitumor Therapies in Advanced Solid Tumors
- Sponsor
- Shanghai Hengrui Pharmaceutical Co., Ltd.
- Study ID
- NCT06895928
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Advanced Solid Tumors
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- SHR-A2102 — DRUGSHR-A2102 for injection.
- Bevacizumab Injection — DRUGBevacizumab injection.
- Adebelimab Injection — DRUGAdebelimab injection.
- Ametinib Mesylate Tablets — DRUGAmetinib mesylate tablets.
- Osimertinib Mesylate Tablets — DRUGOsimertinib mesylate tablets.
Study Details
The study is being conducted to evaluate the safety, tolerability and efficacy of SHR-A2102 with other antitumor therapies in advanced solid tumors to explore the reasonable dosage, safety and efficacy of SHR-A2102 for advanced solid tumors.
Key Dates
- Start date
- Mar 28, 2025
- Status verified
- Mar 2025
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 400 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment Group
Primary Outcome Measure
Adverse events (AEs) [ Time Frame: From day 1 to 90 days after the last dose. ]
Central Contacts
- Yang Wu+86-0518-82342973
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