Ireland
--:--IST
Priya Life Science Compound trial record
Compound · clinical trials

SG301 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our China register that name SG301 as an intervention. Synced 10 Nov 2026
5Current trials
3Recruiting now
2Lead sponsors
1Country register
At a glance

SG301 is named as an intervention in 5 current clinical trials in our China register. 3 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Hangzhou Sumgen Biotech Co., Ltd (4). The most-studied condition is Relapsed or Refractory Multiple Myeloma.

Patient leaflets for SG301

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting360%
  • Not yet open120%
  • Active, closed120%

Trials by phase

  • Phase 2360%
  • Phase 1120%
  • Phase 3120%
01

Clinical trials of SG301

5 trials
StudyPhaseStatusLead sponsorRegisters
A Clinical Study Comparing SG301 Plus Pomalidomide and Dexamethasone to Placebo Plus Pomalidomide and Dexamethasone in Relapsed or Refractory Multiple Myeloma Patients
NCT06508983 · ClinicalTrials.gov ↗ · Relapsed/Refractory Multiple Myeloma
Phase 3 Recruiting Hangzhou Sumgen Biotech Co., Ltd China
A Study of Anti-CD38 Monoclonal Antibody (SG301) Subcutaneous Injection in Children With Nephrotic Syndrome With Frequent Relapses or Steroid Dependence
NCT07087314 · ClinicalTrials.gov ↗ · Nephrotic Syndrome in Children
Phase 2 Recruiting Mao Jianhua China
To Evaluate the Efficacy and Safety of SG301 SC Injection in Systemic Lupus Erythematosus
NCT07447986 · ClinicalTrials.gov ↗ · Systemic Lupus Erythematosus (SLE)
Phase 2 Recruiting Hangzhou Sumgen Biotech Co., Ltd China
Study of SG301 for Renal AMR After Transplantation
NCT07764627 · ClinicalTrials.gov ↗ · Antibody Mediated Rejection
Phase 2 Not yet open Hangzhou Sumgen Biotech Co., Ltd China
SG301 Safety Study in Subjects With Relapsed or Refractory Multiple Myeloma and Other Hematological Malignancies
NCT04684108 · ClinicalTrials.gov ↗ · Relapsed or Refractory Multiple Myeloma, Hematological Malignancy
Phase 1 Active, closed Hangzhou Sumgen Biotech Co., Ltd 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. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with SG301

6 conditions
Relapsed or Refractory Multiple Myeloma1Hematological Malignancy1Nephrotic Syndrome in Children1Antibody Mediated Rejection1Relapsed/Refractory Multiple Myeloma1Systemic Lupus Erythematosus (SLE)1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Hangzhou Sumgen Biotech Co., Ltd4
Mao Jianhua1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China53

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

05

Related compounds

06

Questions about SG301 trials

How many clinical trials are testing SG301?

5 current trials in our China register name SG301 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are SG301 trials recruiting patients?

Yes. 3 of the 5 trials are recruiting: 3 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors SG301 clinical trials?

Hangzhou Sumgen Biotech Co., Ltd (4) and Mao Jianhua (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how SG301 works or whether it is effective, and it is not medical advice.

Approvals, shortages and trials, every Friday

One email a week with new EMA and FDA approvals, EU and US medicine shortages, how many trials are recruiting in Ireland, and the week's Irish pharma news.

Free. Unsubscribe from any email with one click. See our privacy policy.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how SG301 works or whether it is effective. 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 country trial registers, collects every trial that lists SG301 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. 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 ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

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.