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Excyte Biopharma clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China register with Excyte Biopharma as lead sponsor. Synced 26 Sep 2026
6Current trials
5Recruiting 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

Excyte Biopharma is the lead sponsor of 6 current clinical trials in our China register. 5 are recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are YK012 and YKST02. The most-studied condition is Primary Membranous Nephropathy.

ClinicalTrials.gov trials by status

  • Recruiting583%
  • Not yet open117%

Trials by phase

  • Phase 1350%
  • Phase 1/2233%
  • Phase 2117%
01

Clinical trials sponsored by Excyte Biopharma

6 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Study of YK012 in Primary Membranous Nephropathy
NCT06982729 · ClinicalTrials.gov ↗ · Primary Membranous Nephropathy
Drug: YK012
Phase 1 Recruiting 2025-03 China
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of YK012
NCT06565689 · ClinicalTrials.gov ↗ · Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma
Drug: YK012
Phase 1 Recruiting 2023-05 China
Study of YK012 in B-cell Acute Lymphoblastic Leukemia
NCT06580301 · ClinicalTrials.gov ↗ · B-cell Acute Lymphoblastic Leukemia
Drug: YK012
Phase 1/2 Recruiting 2024-09 China
Study of YK012 in Moderate to Severe Systemic Lupus Erythematosus
NCT07010835 · ClinicalTrials.gov ↗ · Systemic Lupus Erythematosus (SLE)
Drug: YK012
Phase 1/2 Recruiting 2025-08 China
A Study of YKST02 in Participants With Relapsed or Refractory Multiple Myeloma
NCT06574568 · ClinicalTrials.gov ↗ · Relapsed or Refractory Multiple Myeloma
Drug: YKST02
Phase 1 Recruiting 2024-06 China
Study of YKST02 in Adults With Relapsed or Refractory Multiple Myeloma
NCT07695740 · ClinicalTrials.gov ↗ · Relapsed or Refractory Multiple Myeloma (RRMM)
Drug: YKST02
Phase 2 Not yet open 2026-09 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 Excyte Biopharma 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 Excyte Biopharma trials

6 conditions
Primary Membranous Nephropathy1Relapsed or Refractory Multiple Myeloma (RRMM)1Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma1B-cell Acute Lymphoblastic Leukemia1Systemic Lupus Erythematosus (SLE)1Relapsed or Refractory Multiple Myeloma1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China65

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

05

Other sponsors in Primary Membranous Nephropathy

SponsorTrials
First Affiliated Hospital, Sun Yat-Sen University2
Shanghai Jiaolian Drug Research and Development2
BioRay Pharmaceutical2
Climb Bio1
Shenzhen Fosun Kairos Biotechnology1

Sponsors with the most current trials registered for this condition.

06

Questions about Excyte Biopharma trials

How many clinical trials does Excyte Biopharma sponsor?

Excyte Biopharma is the lead sponsor of 6 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 Excyte Biopharma trials recruiting?

Yes. 5 of its 6 ClinicalTrials.gov trials are 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 Excyte Biopharma testing?

Its current trials name 2 drugs and biologicals as interventions. The most frequent are YK012 (4) and YKST02 (2). 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.