Skip to main content

luveltamab tazevibulin

Generic: Luveltamab Tazevibulin

luveltamab tazevibulin: developed by 1 company · 6 clinical trials tracked.

luveltamab tazevibulin evidence translation

What we can confirm

What it means

Source-backed records connect luveltamab tazevibulin to STRO; 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 luveltamab tazevibulin → STRO affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 1 study sponsors
Development Pipeline (2)
Clinical Trials (6)

A Phase 1/2, Open-label Study Evaluating the Efficacy, Safety, and Pharmacokinetics (PK) of Luveltamab Tazevibulin (STRO-002) in Infants and Children < 12 Years of Age With CBFA2T3::GLIS2 Acute Myeloid Leukemia (AML)

NCT06679582·Phase 1·STRO
Terminated

Primary endpoint: Evaluate efficacy of luveltamab tazevibulin monotherapy

InterventionalRandomizedopen24 targetStarted 2024-12Completion 2025-0636 sites · Austria, Canada, Denmark, France…Sutro Biopharma, Inc.

A Phase 2, Open-label Study Evaluating STRO-002, an Anti-folate Receptor Alpha (FOLR1) Antibody-Drug Conjugate, in Subjects With Previously Treated Advanced or Metastatic Non-small Cell Lung Cancer Expressing FOLR1

NCT06555263·Phase 2·STRO
Withdrawn

Primary endpoint: Objective Response Rate (ORR)

Interventionalopen0 targetStarted 2024-08Completion 2025-057 sites · United StatesSutro Biopharma, Inc.

A Phase I/IIa Study to Evaluate the Safety, Tolerability , Pharmacokinetics and Preliminary Efficacy of STRO-002 in Chinese Adults With Advanced Epithelial Ovarian Cancer, Endometrial Cancer, and Other Advanced Malignant Solid Tumors.

NCT06238687·Phase 1/Phase 2·CYIG
Completed

Primary endpoint: DLT Assessment

Interventionalopen19 enrolledStarted 2023-11Completion 2025-121 site · ChinaTasly Pharmaceutical Group Co., Ltd

REFRaME-O1: A Phase 2/3 Open-label Study Evaluating the Efficacy and Safety of Luveltamab Tazevibulin (STRO-002) Versus Investigator's Choice (IC) Chemotherapy in Women With Relapsed Platinum-resistant Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers) Expressing Folate Receptor Alpha (FOLR1)

NCT05870748·Phase 2·STRO
Terminated

Primary endpoint: Progression Free Survival (PFS)

InterventionalRandomizedopen600 targetStarted 2023-07Completion 2025-0850 sites · Australia, Canada, Israel, United StatesSutro Biopharma, Inc.

A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-002, an Anti-Folate Receptor Alpha Antibody Drug Conjugate, in Combination With Bevacizumab in Patients With Advanced Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers)

NCT05200364·Phase 1·STRO
Terminated

Primary endpoint: Part 1 - Safety and tolerability of STRO-002/bevacizumab as a combination therapy

Interventionalopen58 targetStarted 2022-03Completion 2025-066 sites · United StatesSutro Biopharma, Inc.

A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-002, an Anti-Folate Receptor Alpha (FolRα) Antibody-Drug Conjugate (ADC), in Patients With Advanced Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers) and Endometrial Cancers

NCT03748186·Phase 1·STRO
Completed

Primary endpoint: Part 1: Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability of STRO-002)

Interventionalopen136 enrolledStarted 2019-02Completion 2024-0627 sites · Spain, United StatesSutro Biopharma, Inc.

Frequently asked questions

Who is developing luveltamab tazevibulin?

luveltamab tazevibulin is being developed by SUTRO BIOPHARMA, INC..

How many clinical trials involve luveltamab tazevibulin?

BioSniper tracks 6 clinical trials involving luveltamab tazevibulin.