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NCT05918107

A Study of PM8002 Injection in Combination With Standard Chemotherapy as First Line Therapy in MPM

Recruiting now Phase 2 Last updated 27 June 2023
What this trial tests

Phase 2 trial testing PM8002 in MPM in 55 participants. Currently enrolling.

Timeline
13 August 2022
Primary endpoint
30 June 2026
30 June 2026

Quick facts

Lead sponsorBiotheus Inc.
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment55
Start date13 August 2022
Primary completion30 June 2026
Estimated completion30 June 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Biotheus Inc. — full company profile →

Who can join

18 and older, any sex, with MPM. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

PM8002 is a bispecific antibody targeting PD-L1 and VEGF. This study will evaluate the efficacy and safety of PM8002 in combination with pemetrexed and platinum as first line treatment for MPM.

Publications & conference data

3 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Bispecific Antibodies in Solid Tumors: Advances and Challenges.
    Shan KS, Musleh Ud Din S, Dalal S, Gonzalez T, et al · · 2025 · cited 12× · PMID 40565299 · DOI 10.3390/ijms26125838
  2. Ivonescimab and other anti-programmed death-1/ligand 1 (PD-(L)1)/vascular endothelial growth factor (VEGF) bispecific antibodies: progress and prospects in cancer therapy.
    Dong C, Wang X. · · 2026 · PMID 42145657 · DOI 10.1093/abt/tbag016
  3. From biology to therapy: current standards and emerging strategies in pleural mesothelioma.
    van Genugten JHLT, de Gooijer CJ, Baas P. · · 2026 · PMID 41971442 · DOI 10.3389/fonc.2026.1778121

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Other trials of PM8002

Trials testing the same drug.

Other Biotheus Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05918107.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing