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taletrectinib

Generic: taletrectinib·Brand: Ibtrozi

taletrectinib: developed by 1 company · 7 clinical trials tracked.

taletrectinib evidence translation

What we can confirm

7 tracked trials

What it means

Source-backed records connect taletrectinib to NUVB; that link alone does not prove the drug works.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

How could taletrectinib → NUVB affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 0 study sponsors

Related indications

Non Small Cell Lung Cancer; Non-small Cell Lung Cancer (NSCLC); Healthy Adult ParticipantsAdult patients with locally advanced or metastatic ROS1-positive ("ROS1+") non-small cell lung cancer ("NSCLC")CarcinomaHealthy Adult ParticipantsLung DiseasesLung NeoplasmsNeoplasmsNeoplasms by Site

Study sponsors

No additional listed-company sponsor is linked.

Development Pipeline (2)
CompanyPhase
Nuvation Bio Inc. (NUVB)
Non Small Cell Lung Cancer; Non-small Cell Lung Cancer (NSCL…
Phase 3
Nuvation Bio Inc. (NUVB)
Adult patients with locally advanced or metastatic ROS1-posi…
Approved
Clinical Trials (7)

Expanded Access Program of Taletrectinib in Patients With Advanced or Metastatic ROS1-Positive NSCLC

No longer available
Expanded AccessNuvation Bio Inc.

An Open-label, Fixed Sequence Study to Evaluate the Effect of Famotidine on the Pharmacokinetics and Safety of Taletrectinib in Healthy Adult Participant

NCT07742384·Phase 1·NUVB
Not yet recruiting

Primary endpoint: Cmax of Taletrectinib

Interventionalopen56 targetStarted 2026-08Completion 2027-02Nuvation Bio Inc.

A Phase 3 Multicenter Double-blind Randomized Study of Taletrectinib Versus Placebo in Patients With ROS1-Fusion Positive Stage IB-IIIA Non-Small Cell Lung Cancer Who Have Undergone Complete Tumor Resection

NCT07154706·Phase 3·NUVB
Recruiting

Primary endpoint: Primary Outcome Measure: To compare the efficacy of taletrectinib with that of placebo, as measured by disease-free survival (DFS) by investigator assessment.

InterventionalRandomizedtriple180 targetStarted 2025-08Completion 2033-0833 sites · Canada, China, United StatesNuvation Bio Inc.

A Phase 3 Multicenter Open-label Study of Taletrectinib Versus a Standard of Care ROS1-Tyrosine Kinase Inhibitor (Crizotinib) in TKI-Naïve Patients With ROS1-Positive Locally Advanced or Metastatic Non-Small Cell Lung Cancer (TRUST-III)

NCT06564324·Phase 3·NUVB
Recruiting

Primary endpoint: PFS (Assessed by BIRC)

InterventionalRandomizedopen194 targetStarted 2024-11Completion 2030-0929 sites · ChinaNuvation Bio Inc.

A Single-Arm, Open-Label, Multicenter Phase 2 Study to Evaluate the Efficacy and Safety of Taletrectinib in Patients With Advanced or Metastatic ROS1 Positive NSCLC and Other Solid Tumors

NCT04919811·Phase 2·NUVB
Active, not recruiting

Primary endpoint: Objective response rate (ORR) by independent radiology review committee (IRC)

Interventionalopen217 targetStarted 2021-09Completion 2027-1250 sites · Canada, China, France, Italy…Nuvation Bio Inc.

A Phase II, Multicenter, Open, Basket Study of AB-106 to Treat the Subjects With Local Progression or Systemic Metastasis Solid Tumors With NTRK Gene Fusion

NCT04617054·Phase 2·NUVB
Terminated

Primary endpoint: Objective response rate (ORR)

Interventionalopen14 targetStarted 2021-06Completion 2024-121 site · ChinaNuvation Bio Inc.

A Multicenter, Open Label, Single Arm Phase 2 Study of AB-106 in the Treatment of Locally Advanced and Metastatic NSCLC

NCT04395677·Phase 2·NUVB
Active, not recruiting

Primary endpoint: Best overall response (BOR) by IRC

Interventionalopen173 targetStarted 2020-07Completion 2027-061 site · ChinaNuvation Bio Inc.

Frequently asked questions

Who is developing taletrectinib?

taletrectinib is being developed by Nuvation Bio Inc..

How many clinical trials involve taletrectinib?

BioSniper tracks 7 clinical trials involving taletrectinib.