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Bisirna Therapeutics (Suzhou) clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China register with Bisirna Therapeutics (Suzhou) as lead sponsor. Synced 26 Sep 2026
3Current trials
0Recruiting now
2Drugs in these trials
1Trial register
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

Bisirna Therapeutics (Suzhou) is the lead sponsor of 3 current clinical trials in our China register. None of its ClinicalTrials.gov trials is recruiting at the moment. The most common phase is Phase 1. The drugs named most often in its trials are VSA012 and Eculizumab. The most-studied condition is Healthy Volunteers.

ClinicalTrials.gov trials by status

  • Not yet open133%
  • Active, closed267%

Trials by phase

  • Phase 1267%
  • Phase 3133%
01

Clinical trials sponsored by Bisirna Therapeutics (Suzhou)

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Multicenter, Randomized, Open-Label, Positive Controlled Phase III Study to Evaluate the Efficacy and Safety of VSA012 Injection in Participants With Paroxysmal Nocturnal Hemoglobinuria Who Are Naive to Complement Inhibitor Therapy
NCT07816237 · ClinicalTrials.gov ↗ · Paroxysmal Nocturnal Hemoglobinuria, PNH
Phase 3 Not yet open 2026-10 China
A Phase I Clinical Study of VSA012 in Healthy Volunteers
NCT06766929 · ClinicalTrials.gov ↗ · Healthy Volunteers
Drug: VSA012
Phase 1 Active, closed 2025-01 China
Safety, PK, and PD of BSA204 in Chinese Adults With Borderline Elevated Lipoprotein(a)
NCT07551505 · ClinicalTrials.gov ↗ · Dyslipidemias
Phase 1 Active, closed 2026-04 China

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 Bisirna Therapeutics (Suzhou) trials

2 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 Bisirna Therapeutics (Suzhou) trials

3 conditions
Healthy Volunteers1Paroxysmal Nocturnal Hemoglobinuria, PNH1Dyslipidemias1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China30

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

05

Other sponsors in Healthy Volunteers

SponsorTrials
Sanofi8
Vigonvita Life Sciences6
Bristol-Myers Squibb5
Hunan Kelun Pharmaceutical4
Shanghai Minwei Biotechnology3
Alnylam Pharmaceuticals2
Karuna Therapeutics, Inc., a Bristol Myers Squibb company2
Sanofi Pasteur, a Sanofi Company2
American Laboratory Products Company2
Xidian University2

Sponsors with the most current trials registered for this condition.

06

Questions about Bisirna Therapeutics (Suzhou) trials

How many clinical trials does Bisirna Therapeutics (Suzhou) sponsor?

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

Are Bisirna Therapeutics (Suzhou) trials recruiting?

Not at the moment. None of its 3 ClinicalTrials.gov trials is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Which drugs is Bisirna Therapeutics (Suzhou) testing?

Its current trials name 2 drugs and biologicals as interventions. The most frequent are VSA012 (2) and Eculizumab (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.