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tara-002

tara-002: developed by 1 company · 3 clinical trials tracked.

tara-002 evidence translation

What we can confirm

What it means

Source-backed records connect tara-002 to TARA; 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 tara-002 → TARA affect its developer, and what evidence supports the link?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 0 study sponsors

Related indications

Lymphatic Malformation; Non-muscle Invasive Bladder Cancer; Bladder (Urothelial, Transitional Cell) CancerBladder (Urothelial, Transitional Cell) Cancer

Study sponsors

No additional listed-company sponsor is linked.

Development Pipeline (1)
CompanyPhase
Protara Therapeutics, Inc. (TARA)
Lymphatic Malformation; Non-muscle Invasive Bladder Cancer; …
Phase 2
Clinical Trials (3)

A Phase 3, Randomized Study to Evaluate the Efficacy and Safety of Intravesical TARA-002 Compared With Investigator's Choice of Intravesical Chemotherapy in Participants With BCG-naïve High-Grade Non-Muscle Invasive Bladder Cancer

NCT07480356·Phase 3·TARA
Recruiting

Primary endpoint: Incidence of high-grade complete response

InterventionalRandomizedopen284 targetStarted 2026-05Completion 2032-1110 sites · Ukraine, United StatesProtara Therapeutics

A Phase 2a/b Single Arm Open Label Study to Evaluate the Safety and Efficacy of Intracystic Administration of TARA-002 in Participants Between 6 Months to Less Than 18 Years of Age for the Treatment of Macrocystic and Mixed Cystic Lymphatic Malformations

NCT05871970·Phase 2·TARA
Recruiting

Primary endpoint: Proportion of participants with clinical success after one treatment cycle of TARA-002

Interventionalopen38 targetStarted 2023-10Completion 2027-0511 sites · United StatesProtara Therapeutics

A Phase 2, Open-Label Study to Evaluate the Safety and Efficacy of Intravesical Instillation of TARA-002 in Adults With High-Grade Non-Muscle Invasive Bladder Cancer

NCT05951179·Phase 2·TARA
Recruiting

Primary endpoint: Cohort A and B: Incidence of high-grade Complete Response at any time according to central pathology after treatment with TARA-002

Interventionalopen131 targetStarted 2023-09Completion 2032-0350 sites · Argentina, United StatesProtara Therapeutics

Frequently asked questions

Who is developing tara-002?

tara-002 is being developed by Protara Therapeutics, Inc..

How many clinical trials involve tara-002?

BioSniper tracks 3 clinical trials involving tara-002.