Study of Iparomlimab and Tuvonralimab Plus Chemotherapy in Malignant Mesothelioma

PHASE1/PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

55

Participants

Timeline

Start Date

September 1, 2025

Primary Completion Date

October 31, 2026

Study Completion Date

July 1, 2027

Conditions
Malignant MesotheliomaMesothelioma
Interventions
DRUG

iparomlimab 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)"

All Listed Sponsors
collaborator

Qilu Pharmaceutical Co., Ltd.

INDUSTRY

collaborator

Affiliated Cancer Hospital of Zhengzhou University

UNKNOWN

collaborator

Beijing Chest Hospital, Capital Medical University

OTHER

collaborator

The Affiliated Hospital of Inner Mongolia Medical University

OTHER

collaborator

Shaanxi Provincial Cancer Hospital

OTHER

lead

National Cancer Center, China

OTHER