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NCT04478461

Safety, Tolerability, and Pharmacokinetics of MW11 in Patients With Advanced Solid Tumors

Status unknown Phase 1 Last updated 13 November 2020
What this trial tests

Phase 1 trial testing PD-1 monoclonal antibody in Advanced Solid Tumor in 21 participants. Status unknown.

Timeline
3 September 2020
Primary endpoint
5 January 2023
2 February 2023

Quick facts

Lead sponsorMabwell (Shanghai) Bioscience Co., Ltd.
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment21
Start date3 September 2020
Primary completion5 January 2023
Estimated completion2 February 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Mabwell (Shanghai) Bioscience Co., Ltd. — full company profile →

Who can join

Adults 18 to 75, any sex, with Advanced Solid Tumor. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase Ia, single-center, open label, dose escalation clinical study to evaluate the safety, tolerability, pharmacokinetics, immunogenicity and anti-tumor efficacy of MW11 (a recombinant humanized anti-PD-1 monoclonal antibody) for injection in patients with advanced solid tumors.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Leading Edge: Intratumor Delivery of Monoclonal Antibodies for the Treatment of Solid Tumors.
    Blanco E, Chocarro L, Fernández-Rubio L, Bocanegra A, et al · · 2023 · cited 12× · PMID 36768997 · DOI 10.3390/ijms24032676

Verify or expand the search:

Other trials of PD-1 monoclonal antibody

Trials testing the same drug.

Other recruiting trials for Advanced Solid Tumor

Currently open trials in the same condition.

Other Mabwell (Shanghai) Bioscience Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04478461.

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