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Shenzhen Kexing Pharmaceutical clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our China register with Shenzhen Kexing Pharmaceutical as lead sponsor. Synced 26 Sep 2026
3Current trials
1Recruiting now
1Drug 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

Shenzhen Kexing Pharmaceutical is the lead sponsor of 3 current clinical trials in our China register. 1 is recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are GB18. The most-studied condition is Growth Hormone Deficiency in Children.

ClinicalTrials.gov trials by status

  • Recruiting133%
  • Not yet open267%

Trials by phase

  • Phase 1267%
  • Phase 2/3133%
01

Clinical trials sponsored by Shenzhen Kexing Pharmaceutical

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
To Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of GB18 Injection in Healthy Participants
NCT07237464 · ClinicalTrials.gov ↗ · Cancer Cachexia (CC), Cancer Cachexia, Cancer Cachexia Syndrome
Drug: GB18
Phase 1 Recruiting 2025-10 China
Evaluating the Efficacy and Safety of GB08 Injection in Pediatric Patients With Growth Hormone Deficiency
NCT07126288 · ClinicalTrials.gov ↗ · Growth Hormone Deficiency in Children, Growth Hormone Deficiency (GHD), Growth Hormone
Phase 2/3 Not yet open 2025-08 China
To Evaluate the Safety, Pharmacokinetics, and Efficacy of GB10 Intravitreal Injection in Patients With Neovascular Age-related Macular Degeneration (nAMD)
NCT07406438 · ClinicalTrials.gov ↗ · Neovascular Age-Related Macular Degeneration (nAMD)
Phase 1 Not yet open 2026-02 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 Shenzhen Kexing Pharmaceutical trials

1 compound

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 Shenzhen Kexing Pharmaceutical trials

7 conditions
Growth Hormone Deficiency in Children1Growth Hormone Deficiency (GHD)1Growth Hormone1Cancer Cachexia (CC)1Cancer Cachexia1Cancer Cachexia Syndrome1Neovascular Age-Related Macular Degeneration (nAMD)1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in China31

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

05

Other sponsors in Growth Hormone Deficiency in Children

SponsorTrials
Kexing Biopharm1

Sponsors with the most current trials registered for this condition.

06

Questions about Shenzhen Kexing Pharmaceutical trials

How many clinical trials does Shenzhen Kexing Pharmaceutical sponsor?

Shenzhen Kexing Pharmaceutical 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 Shenzhen Kexing Pharmaceutical 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 Shenzhen Kexing Pharmaceutical testing?

Its current trials name 1 drug or biological as interventions. The most frequent are GB18 (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.