Malignant Mesothelioma, Mesothelioma
Conditions
Keywords
Malignant Mesothelioma, iparomlimab and tuvonralimab, immunotherapy
Brief summary
This clinical trial aims to investigate the effectiveness and safety of a new treatment combination-Iparomlimab and Tuvonralimab (QL1706, a dual-function antibody targeting PD-1 and CTLA-4) combined with chemotherapy-for patients with malignant mesothelioma (MM). MM is a rare and aggressive cancer often linked to asbestos exposure. Current treatments have limited success, and this study seeks to explore a potentially more effective and safer option. Study Design: Phase Ib (Safety Phase): 6 patients will receive the combination therapy to assess safety. If no major safety issues arise, the study will proceed to Phase II. Phase II (Efficacy Phase): 49 patients will be enrolled to evaluate treatment effectiveness. The study includes two groups for first-line treatment and second-line treatment.
Detailed description
Study Rationale Malignant mesothelioma (MM) is a rare and aggressive cancer primarily associated with asbestos exposure. Despite advances in treatment, the prognosis remains poor, with a median overall survival (OS) of approximately 12-18 months for advanced disease. Current standard therapies include platinum-based chemotherapy combined with pemetrexed, immune checkpoint inhibitors (ICIs) such as nivolumab plus ipilimumab, or pembrolizumab with chemotherapy. However, these treatments have limitations, including significant toxicity (e.g., immune-related adverse events, irAEs) and modest survival benefits in certain populations. The iparomlimab and tuvonralimab (QL1706) combination is a novel bispecific antibody therapy targeting PD-1 and CTLA-4, designed to enhance anti-tumor immune responses while minimizing toxicity. Preclinical and early clinical data suggest this dual checkpoint blockade may offer comparable efficacy to existing ICI combinations but with an improved safety profile. Given the unmet need for effective and tolerable therapies in MM, this study evaluates the clinical potential of iparomlimab and tuvonralimab combined with chemotherapy in Chinese patients. Study Design This is a single-arm, multicenter, open-label Ib/II trial with two sequential phases: Phase Ib (Safety Run-In, n=6): Evaluates the safety of iparomlimab and tuvonralimab + chemotherapy in patients with 1-3 prior lines of therapy. Phase II (Expansion, n=49): First-line cohort (n=39): Patients receive iparomlimab and tuvonralimab + pemetrexed/platinum (Simon two-stage design). Second-line cohort (n=10): Fixed-sample evaluation of iparomlimab and tuvonralimab + investigator-selected chemotherapy. Treatment Regimen Induction Phase (4-6 cycles, Q3W): Iparomlimab and tuvonralimab (5 mg/kg IV, Day 1) Chemotherapy backbone: First-line: Pemetrexed (500 mg/m²) + cisplatin (75 mg/m²) or carboplatin (AUC 5). Second-line: Investigator's choice (pemetrexed, gemcitabine, or vinorelbine). Maintenance Phase (up to 2 years, Q3W): Iparomlimab and tuvonralimab monotherapy (5 mg/kg) until progression or unacceptable toxicity.
Interventions
DRUGiparomlimab and tuvonralimab (Dual PD-1/CTLA-4 blockade) + chemotherapy
Novel Bispecific Checkpoint Inhibition: QL1706(iparomlimab and Tuvonralimab) was generated by using MabPair, a new technological platform that enables the production of two antibodies close to their natural forms from a single host cell line and is manufactured as one product. QL1706 contains a mixture of anti-PD-1 IgG4 and anti-CTLA-4 IgG1 that were produced together in a fixed ratio. Each antibody was individually optimized to achieve desirable target coverage and antibody effector functions. Chemotherapy for first-line treatment (pemetrexed plus cisplatin or carboplatin ) Chemotherapy for second-line treatment (pemetrexed, gemcitabine or vinorelbine)
Sponsors
Qilu Pharmaceutical Co., Ltd.
Affiliated Cancer Hospital of Zhengzhou University
Beijing Chest Hospital, Capital Medical University
The Affiliated Hospital of Inner Mongolia Medical University
Shaanxi Provincial Cancer Hospital
National Cancer Center, China
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Subjects must provide informed consent prior to initiating any study-specific procedures. * Male or female subjects aged ≥18 and ≤75 years. * Histologically/cytologically confirmed malignant mesothelioma (MM), including malignant pleural mesothelioma (PM) and malignant peritoneal mesothelioma (PeM). * Subjects with MM unsuitable for radical resection and/or radiotherapy per AJCC 8th Edition. * Subjects who received neoadjuvant/adjuvant chemotherapy for radical surgery completed \>6 months prior to current recurrent disease diagnosis, not counted in subsequent treatment lines. * Prior systemic anti-tumor therapy requirements: * Safety run-in phase: ≥1 prior anti-tumor therapy line (maximum 3 lines) * Phase II first-line cohort: No prior systemic anti-tumor therapy * Phase II second-line cohort: Only 1 prior systemic anti-tumor therapy line * ECOG performance status 0-2. * Investigator-assessed life expectancy \>3 months. * Adequate hematological parameters.
Exclusion criteria
* Prior CTLA-4 inhibitors prohibited; prior PD-1/PD-L1 allowed unless discontinued for immune toxicity * Immunomodulators within 14 days (e.g., thymosin, interleukin-2, interferon) * Significant cardiovascular history within 6 months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ORR | From enrollment to the end of treatment at 8 weeks | Objective Response Rate，Proportion of participants achieving complete response (CR) or partial response (PR) per modified RECIST 1.1 for mesothelioma |
Contacts
Primary ContactPuyuan Xing, MD
Outcome results
None listed