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NCT04389229: OVSTAR

OVSTAR TIL Trial (OVarian Cancer Co-STimulatory Antigen Receptor TIL Trial)

Withdrawn Phase 1, PHASE2 Last updated 16 December 2020
What this trial tests

Phase 1, PHASE2 trial testing cyclophosphamide in Ovarian Cancer Metastatic. Withdrawn.

Timeline
1 July 2020
Primary endpoint
31 March 2023
31 July 2025

Quick facts

Lead sponsorImmetacyte Ltd
PhasePhase 1, PHASE2
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Start date1 July 2020
Primary completion31 March 2023
Estimated completion31 July 2025
Sites2 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Immetacyte Ltd — full company profile →

Who can join

18 and older, female only, with Ovarian Cancer Metastatic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

An open label, multi-centre Phase 1/2a study of modified and unmodified autologous Tumour Infiltrating Lymphocytes (TIL) in patients with platinum-resistant ovarian cancer. The purpose of this phase I/II study is to evaluate the feasibility and safety of both standard unmodified TIL (UTIL-01) and TIL engineered to express the co-stimulatory receptor CoStAR (CoTIL-01) in platinum resistant ovarian cancer.

Publications & conference data

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

  1. Adoptive T cell therapy for ovarian cancer.
    Gitto SB, Ihewulezi CJN, Powell DJ. · · 2024 · cited 16× · PMID 38603955 · DOI 10.1016/j.ygyno.2024.04.001

Verify or expand the search:

Other trials of cyclophosphamide

Trials testing the same drug.

Other recruiting trials for Ovarian Cancer Metastatic

Currently open trials in the same condition.

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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/NCT04389229.

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