A Study of Chidamide Combined With Ivonescimab in the Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC) With Acquired Resistance to Immunotherapy and High Yes-associated Protein (YAP) Expression
- Sponsor
- Guangdong Association of Clinical Trials
- Study ID
- NCT07412262
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Chidamide in combination with Ivonescimab — DRUGChidamide 20mg/dose orally BIW; Ivonescimab 20mg/kg intravenously (IV) Q3W
Study Details
This is a prospective, single-arm, multi-center, phase II clinical trial to evaluate the efficacy and safety of Chidamide in combination with Ivonescimab in the treatment of advanced non-small cell lung cancer with secondary immune resistance and high YAP protein expression.
Key Dates
- Start date
- May 15, 2026
- Status verified
- Jan 2026
- Primary completion
- Mar 31, 2028
- Completion
- Mar 31, 2029
Study Design
- Enrollment
- 32 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: The combination of Chidamide plus Ivonescimab(AK112)Participants will take 20 mg of Chidamide by month every 3-4 days on a twice weekly (BIW) schedule and Ivonescimab (AK112) 20 mg/kg intravenously (IV) Q3W.
Primary Outcome Measure
Progression Free Survival(PFS) per Response Evaluation Criteria in Solid tumors (RECIST) v1.1 [ Time Frame: From the start of treatment until disease progression or death (assessed up to 24 months) ]
Central Contacts
- Qing Zhou, MD+86 02083827812
- Yi-chen Zhang, MD86 19128287863
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