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Priya Life Science Sponsor trial record
Sponsor · clinical trials

Shanghai Fosun Pharmaceutical Industrial Development clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China and Japan registers with Shanghai Fosun Pharmaceutical Industrial Development as lead sponsor. Synced 10 Nov 2026
24Current trials
7Recruiting now
7Drugs in these trials
2Trial registers
At a glance

Shanghai Fosun Pharmaceutical Industrial Development is the lead sponsor of 24 current clinical trials in our China and Japan registers. 7 are recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are Luvometinib, FXS6837 and FXS5626. The most-studied condition is Paroxysmal Nocturnal Hemoglobinuria.

ClinicalTrials.gov trials by status

  • Recruiting729%
  • Not yet open1042%
  • Active, closed521%
  • By invitation28%

Trials by phase

  • Phase 1833%
  • Phase 2729%
  • Phase 3521%
  • Phase 1/228%
  • Phase 2/314%
  • Not applicable14%
01

Clinical trials sponsored by Shanghai Fosun Pharmaceutical Industrial Development

24 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
QT Interval Effects Study of Oral FXS5626 Tablets
NCT07695779 · ClinicalTrials.gov ↗ · Evaluation of QTc Interval
Drug: FXS5626
Phase 1 Recruiting 2026-08 China
A Phase I Study of XS-02 Capsules in Patients With Advanced Solid Tumors
NCT06531486 · ClinicalTrials.gov ↗ · Solid Tumor, Ovarian Cancer, Breast Cancer
Phase 1 Recruiting 2024-08 China
A Study of XS-04 in Patients With Relapsed or Refractory Hematologic Malignancies
NCT06820268 · ClinicalTrials.gov ↗ · B-cell Lymphoma, Acute Myeloid Leukemia, Myelodysplastic Syndrome
Phase 1 Recruiting 2025-01 China
Phase I Study of FXS0683 in the Treatment of Blood Tumors
NCT07616089 · ClinicalTrials.gov ↗ · B-Cell Lymphoma, Acute Myeloid Leukemia, Myelodysplastic Syndromes
Phase 1 Recruiting 2026-06 China
A Phase 2 Study of Luvometinib Combined With Anlotinib in KRAS-mutated NSCLC
NCT07562581 · ClinicalTrials.gov ↗ · Non-small Cell Lung Caner, KRAS-mutated, Metastasis
Phase 2 Recruiting 2026-06 China
A Phase II Clinical Trial to Evaluate the Efficacy and Safety of FXS5626 in Patients With NIU
NCT07552012 · ClinicalTrials.gov ↗ · Active Non-anterior, Non-infectious Uveitis
Drug: FXS5626
Phase 2 Recruiting 2026-01 China
To Evaluate the Efficacy, Safety, and PK Characteristics of FCN-159 in Pediatric Patients With Refractory/Recurrent LCH
NCT05997602 · ClinicalTrials.gov ↗ · Langerhans Cell Histiocytosis, LCH
Phase 2 Recruiting 2023-09 China
Mass Balance Study of [¹⁴C]FXS4640 in Healthy Adult Males
NCT07872579 · ClinicalTrials.gov ↗ · Healthy Subjects
Phase 1 Not yet open 2026-10 China
A Study of Efficacy and Safety of FXS6837 in Anti-C5 Treated PNH Patients.
NCT07914894 · ClinicalTrials.gov ↗ · Paroxysmal Nocturnal Hemoglobinuria
Drug: FXS6837
Phase 3 Not yet open 2027-01 China
Phase II/III Study of FXS5626 in Participants With Non-segmental Vitiligo
NCT07840820 · ClinicalTrials.gov ↗ · Non-segmental Vitiligo
Phase 2/3 Not yet open 2026-10 China
FCN-159 Monotherapy Versus Chemotherapy by Investigator's Choice in Pediatric Low-grade Glioma Patients With BRAF Alteration
NCT07004075 · ClinicalTrials.gov ↗ · Low-grade Glioma, Pediatric Low-grade Gliomas, pLGG With BRAF Alteration
Phase 3 Not yet open 2025-06 China
Phase I Study of FXS887 in the Treatment of Solid Tumors
NCT07345637 · ClinicalTrials.gov ↗ · Solid Tumor Refractory to Conventional Treatment
Phase 1 Not yet open 2026-01 China
A Study of the Efficacy and Safety of FXS6837 Capsules Compared to Eculizumab for 24 Weeks in Patients With PNH.
NCT07747090 · ClinicalTrials.gov ↗ · Paroxysmal Nocturnal Hemoglobinuria
Phase 3 Not yet open 2026-12 China
FXS6837 for the Treatment for IgAN Patients(Longterm Study)
NCT07750665 · ClinicalTrials.gov ↗ · Primary IgAN
Drug: FXS6837
Phase 2 Not yet open 2026-09 China
FXS6837 for the Treatment of IgAN Patients
NCT07502638 · ClinicalTrials.gov ↗ · IgAN
Phase 2 Not yet open 2026-03 China
Follow-up Study to Evaluate the Safety and Efficacy of FCN-159 in Pediatric Participants With Neurofibromatosis Type 1
NCT07024394 · ClinicalTrials.gov ↗ · Neurofibromatosis 1, Plexiform Neurofibroma, NF1
Phase 1/2 Not yet open 2025-06 China
Phase Ia/Ib Study of FXB0871 Monotherapy in Locally Advanced/Metastatic Solid Tumors
NCT07558200 · ClinicalTrials.gov ↗ · Solid Tumors, Non-Small Cell Lung Cancer, Hepatocellular Carcinoma
Drug: TEV-56278
Phase 1 Not yet open 2026-05 China
A Multicenter, Open-label Study Evaluating the Long-term Safety and Efficacy of XH-S003 Capsules in Patients With Paroxysmal Nocturnal Hemoglobinuria
NCT07657052 · ClinicalTrials.gov ↗ · Paroxysmal Nocturnal Hemoglobinuria
Drug: XH-S003
Not applicable By invitation 2025-08 China
XS-03 in Combination With FOLFOX or FOLFIRI and Bevacizumab for Treatment of Metastatic Colorectal Cancer Patients With RAS Mutation
NCT06936527 · ClinicalTrials.gov ↗ · Colorectal Cancer, Metastatic Colorectal Cancer With RAS Mutation
Phase 1/2 By invitation 2025-05 China
The Phase Ib Clinical Trial of the XH-S004 Tablet in Patients With Chronic Obstructive Pulmonary Disease (COPD) to Evaluate Its Safety, Tolerability, Pharmacokinetic Characteristics and Pharmacodynamic Characteristics After Multiple Administrations
NCT07035652 · ClinicalTrials.gov ↗ · Chronic Obstructive Pulmonary Disease
Phase 1 Active, closed 2025-07 China, Japan
A Multicenter, Randomized, Double-blind, Placebo-controlled Parallel-group Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of XH-S004 Tablets in Patients With Non-cystic Fibrosis Bronchiectasis
NCT06981091 · ClinicalTrials.gov ↗ · Non-Cystic Fibrosis Bronchiectasis
Phase 2 Active, closed 2025-05 China
FCN-159 in Adult Patients With Symptomatic, Inoperable Neurofibromatosis Type 1-Related Plexiform Neurofibromas
NCT05913037 · ClinicalTrials.gov ↗ · Neurofibromatosis 1, Plexiform Neurofibroma, NF1
Phase 3 Active, closed 2023-06 China
FCN-338 in Combination With Azacitidine or Chemotherapy in Myeloid Neoplasms
NCT06858618 · ClinicalTrials.gov ↗ · Safety, Antitumor Activity, PK Profile
Phase 2 Active, closed 2023-08 China
Study Of Comparing SAF-189s With Crizotinib In First Line ALK-Positive Advanced and Metastatic NSCLC
NCT06569420 · ClinicalTrials.gov ↗ · Non-Small Cell Lung Cancer, ALK-positive, SAF-189s
Phase 3 Active, closed 2021-12 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 Shanghai Fosun Pharmaceutical Industrial Development trials

7 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 Shanghai Fosun Pharmaceutical Industrial Development trials

42 conditions
Paroxysmal Nocturnal Hemoglobinuria3Acute Myeloid Leukemia2Neurofibromatosis 12Plexiform Neurofibroma2NF12Non-Small Cell Lung Cancer2Healthy Subjects1Evaluation of QTc Interval1Solid Tumor1Ovarian Cancer1Breast Cancer1Endometrial Cancer1Chronic Obstructive Pulmonary Disease1Non-segmental Vitiligo1B-cell Lymphoma1Myelodysplastic Syndrome1Low-grade Glioma1Pediatric Low-grade Gliomas1pLGG With BRAF Alteration1Solid Tumor Refractory to Conventional Treatment1B-Cell Lymphoma1Myelodysplastic Syndromes1Acute Lymphoblastic Leukemia1Non-Cystic Fibrosis Bronchiectasis1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China247
Clinical trials in Japan10

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

05

Other sponsors in Paroxysmal Nocturnal Hemoglobinuria

SponsorTrials
Alexion Pharmaceuticals4
Nanjing Chia-tai Tianqing Pharmaceutical3
Longbio Pharma1
Chengdu Suncadia Medicine1

Sponsors with the most current trials registered for this condition.

06

Questions about Shanghai Fosun Pharmaceutical Industrial Development trials

How many clinical trials does Shanghai Fosun Pharmaceutical Industrial Development sponsor?

Shanghai Fosun Pharmaceutical Industrial Development is the lead sponsor of 24 current trials on ClinicalTrials.gov in our China and Japan registers, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Shanghai Fosun Pharmaceutical Industrial Development trials recruiting?

Yes. 7 of its 24 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 Shanghai Fosun Pharmaceutical Industrial Development testing?

Its current trials name 7 drugs and biologicals as interventions. The most frequent are Luvometinib (4), FXS6837 (3), FXS5626 (2), Anlotinib (1) 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 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.