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NCT06980077PHASE2RECRUITING

Ivonescimab for the Treatment of Thymic Cancer

UCLA L-11: A Phase II Trial of Ivonescimab for Previously Treated Thymic Carcinoma

Sponsor: Jonsson Comprehensive Cancer Center + Summit Therapeutics

No open prediction endpoints

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Key Facts

Study type
INTERVENTIONAL
Conditions
Thymus Carcinoma
Interventions
Biopsy Procedure, Biospecimen Collection, Computed Tomography, Ivonescimab
Enrollment
25 participants
Primary completion
Jun 2027
Study completion
Jun 2028
First posted
May 2025
Last updated
Oct 2025

Primary Endpoints (CT.gov)

Overall response rate (ORR)

Time frame: Up to 1 year

Secondary Endpoints

Progression free survival

Duration of response

Time to response

Eligibility Criteria

Inclusion Criteria: * Male or female ≥ 18 years of age and willing and able to provide informed consent * Cytologically or histologically confirmed thymic carcinoma, which is incurable * Received prior systemic therapy for thymic carcinoma, or is ineligible for or refuses other therapies * Measurable disease, as per RECIST 1.1 * Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 * Absolute neutrophil count (ANC) ≥ 1.5 × 10\^9/L * Platelets ≥ 100 × 10\^9/L * Hemoglobin ≥ 9 g/dL or ≥ 5.6 mmol/L * Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated creatinine clearance (CrCl) ≥ 50 mL/min (glomerular filtration rate \[GFR\] can also be used in place of creatinine or CrCl) * Estimated glomerular filtration rate (eGFR) value ≥ 50 mL/min for participants with creatinine levels \> 1.5 x institutional ULN * Creatinine clearance may be calculated using the Cockcroft-Gault formula or estimated glomerular filtration rate (eGFR) may be calculated us

Read full criteria on CT.gov →

✦ Analyst Commentary

Expert commentary on why this trial matters and what to watch for.

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Source

Open on ClinicalTrials.gov