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Transcenta Therapeutics (Hangzhou) clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our USA and China registers with Transcenta Therapeutics (Hangzhou) as lead sponsor. Synced 26 Sep 2026
3Current trials
1Recruiting now
10Drugs in these trials
2Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Transcenta Therapeutics (Hangzhou) is the lead sponsor of 3 current clinical trials in our USA and China registers. 1 is recruiting patients now. All registered phases are Phase 1/2. The drugs named most often in its trials are Gemcitabine, Nivolumab and TST001. The most-studied condition is Advanced Cancer.

ClinicalTrials.gov trials by status

  • Recruiting133%
  • Active, closed267%

Trials by phase

  • Phase 1/23100%
01

Clinical trials sponsored by Transcenta Therapeutics (Hangzhou)

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Trial to Evaluate Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of TST001 in Advanced or Metastatic Solid Tumors
NCT04495296 · ClinicalTrials.gov ↗ · Advanced Cancer
Phase 1/2 Recruiting 2020-08 China
A First-in-Human, Phase 1 Study of TST003 in Subjects With Solid Tumors
NCT05731271 · ClinicalTrials.gov ↗ · Locally Advanced Solid Tumor, Metastatic Tumor, Colorectal Adenocarcinoma
Phase 1/2 Active, closed 2023-02 USA
A Trial to Evaluate Safety and Tolerability of TST001 in Advanced or Metastatic Solid Tumors
NCT04396821 · ClinicalTrials.gov ↗ · Advanced Cancer, Gastric Cancer, Gastroesophageal-junction Cancer
Phase 1/2 Active, closed 2020-05 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Drugs in Transcenta Therapeutics (Hangzhou) trials

10 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in Transcenta Therapeutics (Hangzhou) trials

7 conditions
04

By trial register

RegisterTrialsRecruiting
Clinical trials in USA20
Clinical trials in China11

A trial with sites in more than one country appears in each of those registers.

05

Other sponsors in Advanced Cancer

SponsorTrials
Chia Tai Tianqing Pharmaceutical Group3
Mirati Therapeutics2
Arcus Biosciences2
Agenus1
MacroGenics1
Solve Therapeutics1
Biocity Biopharmaceutics1
HC Biopharma1

Sponsors with the most current trials registered for this condition.

06

Questions about Transcenta Therapeutics (Hangzhou) trials

How many clinical trials does Transcenta Therapeutics (Hangzhou) sponsor?

Transcenta Therapeutics (Hangzhou) is the lead sponsor of 3 current trials on ClinicalTrials.gov in our USA and China registers, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Transcenta Therapeutics (Hangzhou) trials recruiting?

Yes. 1 of its 3 ClinicalTrials.gov trials is recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Transcenta Therapeutics (Hangzhou) testing?

Its current trials name 10 drugs and biologicals as interventions. The most frequent are Gemcitabine (2), Nivolumab (2), TST001 (2), Albumin-Bound Paclitaxel (1) and Capecitabine (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.