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NCT05275478CompletedPhase 1/2

Study to see how safe is TNG908 at different doses in patients with solid tumors that have a gene called MTAP missing

A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors

Source: EU CTIS (euclinicaltrials.eu) · Last updated 24 Jul 2025

Brief summary (registry, in English)

"Phase 1: To determine the MTD and RP2D(s) of TNG908 Phase 2: To assess anti-neoplastic activity of TNG908 in patients with MTAP-deleted advanced solid tumors"

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
50 (actual)
First submitted
12 Aug 2024
Start date
31 Oct 2022
Lead sponsor
Tango Therapeutics Inc.
NCT number
NCT05275478
EU CT number
2024-511976-34-00
EudraCT number
2021-005605-27

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 50
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Not have received prior treatment with a PRMT5 inhibitor.

Who the study is looking for

  • "_Age: ≥18 years-of-age at the time of signature of the main study ICF _Performance status: a)Patients with solid tumors other than R/R GBM: ECOG performance status score of 0 to 1 b) Patients with R/R GBM: Karnofsky performance status score ≥70 _For solid tumors other than R/R GBM, have confirmed histologic or cytologic diagnosis of a locally advanced, metastatic, and/or unresectable solid tumor or for GBM, have R/R GBM _Prior standard therapy, as available _Documented bi-allelic (homozygous) deletion of MTAP in a tumor detected by a validated NGS test, or absence of MTAP protein in a tumor detected by a validated IHC test. _Adequate organ function/reserve per local labs _Adequate liver function per local labs _Adequate renal function per local labs _Negative serum pregnancy test result at screening _Patient must be able to swallow tablets _Written informed consent must be obtained according to local guidelines"

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceCompleted
Centre Leon Berard
Coordinator of this site? Confirm its status
LyonFranceCompleted
Institut De Cancerologie De L Ouest
Coordinator of this site? Confirm its status
Saint-Herblain CedexFranceCompleted
Oncopole Claudius Regaud
Coordinator of this site? Confirm its status
Toulouse Cedex 9FranceCompleted
Institut Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceCompleted

This page is information, not medical advice. Discuss any trial with your doctor.