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NCT05821777

A Study to Evaluate Safety, Tolerability and Preliminary Activity of LB101 in Participants With Advanced Solid Tumors

Terminated Phase 1, PHASE2 Last updated 25 September 2025
What this trial tests

Phase 1, PHASE2 trial testing LB101 in Advanced Solid Tumor in 25 participants. Terminated before completion.

Timeline
28 March 2023
Primary endpoint
24 January 2025
9 September 2025

Quick facts

Lead sponsorCentessa Pharmaceuticals (UK) Limited
PhasePhase 1, PHASE2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment25
Start date28 March 2023
Primary completion24 January 2025
Estimated completion9 September 2025
Sites7 locations across France, United States

Drugs / interventions tested

Conditions studied

Sponsor

Centessa Pharmaceuticals (UK) Limited — full company profile →

Who can join

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

Sponsor's own description

The purpose of this study is to assess safety, tolerability, and preliminary activity of LB101 monotherapy in participants with advanced solid tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Advanced Solid Tumor

Currently open trials in the same condition.

Other Centessa Pharmaceuticals (UK) Limited 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/NCT05821777.

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