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Priya Life Science Compound trial record
Compound · clinical trials

Anrikefon clinical trials

Also listed in trial records as HSK21542
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our China register that name Anrikefon as an intervention. Synced 10 Nov 2026
5Current trials
4Recruiting now
5Lead sponsors
1Country register
At a glance

Anrikefon is named as an intervention in 5 current clinical trials in our China register. 4 are recruiting patients now. The most common phase is Phase 4. The sponsor with the most trials is The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School (1). The most-studied condition is Patients Who Undergo Pancreaticoduodenectomy.

How Anrikefon works

All drug targets →
  • Agonist at OPRK1 Primary target
    Target: OPRK1 opioid receptor kappa 1
    Guide to Pharmacology only
Diseases it has been tested for in clinical trials, by furthest phase
  • PruritusPhase 3

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5095089, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 14403, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Anrikefon

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

  • Recruiting480%
  • Not yet open120%

Trials by phase

  • Phase 4360%
  • Phase 2240%
01

Clinical trials of Anrikefon

5 trials
StudyPhaseStatusLead sponsorRegisters
Efficacy and Safety of Anrikefon for Postoperative Analgesia in Ophthalmic Surgery
NCT07269106 · ClinicalTrials.gov ↗ · Ophthalmic Surgery, Postoperative Pain Management, Opioid Analgesia
Phase 4 Recruiting Zhongshan Ophthalmic Center, Sun Yat-sen University China
Anrikefon vs Nalfurafine for Sleep Quality in Hemodialysis Patients With CKD-aP
NCT07380113 · ClinicalTrials.gov ↗ · Pruritus Chronic, Kidney Diseases, Chronic, Renal Insufficiency, Chronic
Phase 4 Recruiting Zhujiang Hospital China
Anrikefon-based Patient-controlled Intravenous Analgesia Following Laparoscopic Surgery
NCT07525986 · ClinicalTrials.gov ↗ · Laparoscopic Surgery, Visceral Pain, Postoperative, Anrikefon
Phase 4 Recruiting Peking University First Hospital China
Safety and Efficacy of Anricfen for Postoperative Analgesia and Rehabilitation Promotion After Pancreaticoduodenectomy.Intervention Measures: For Normal Adults, Administer Ariceptin Injection Intravenously Post-operation at a Dose of 1 μg/Kgevery 8 Hours for Three Consecutive Days After Surgery.
NCT07514637 · ClinicalTrials.gov ↗ · Patients Who Undergo Pancreaticoduodenectomy
Phase 2 Recruiting The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School China
A Study on the Efficacy and Safety of Anrikefon for Postoperative Pain Relief Following Laparoscopic Cholecystectomy
NCT07741188 · ClinicalTrials.gov ↗ · Gallbladder Stones, Gallbladder Polyps
Phase 2 Not yet open Affiliated Hospital of Guangdong Medical University 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 Anrikefon

14 conditions
Patients Who Undergo Pancreaticoduodenectomy1Pruritus Chronic1Kidney Diseases, Chronic1Renal Insufficiency, Chronic1Uremia; Chronic1Gallbladder Stones1Gallbladder Polyps1Laparoscopic Surgery1Visceral Pain, Postoperative1Anrikefon1Patient-controlled Intravenous Analgesia1Ophthalmic Surgery1
All 14 conditions
Condition (as registered)Trials
Patients Who Undergo Pancreaticoduodenectomy1
Pruritus Chronic1
Kidney Diseases, Chronic1
Renal Insufficiency, Chronic1
Uremia; Chronic1
Gallbladder Stones1
Gallbladder Polyps1
Laparoscopic Surgery1
Visceral Pain, Postoperative1
Anrikefon1
Patient-controlled Intravenous Analgesia1
Ophthalmic Surgery1
Postoperative Pain Management1
Opioid Analgesia1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School1
Zhujiang Hospital1
Affiliated Hospital of Guangdong Medical University1
Peking University First Hospital1
Zhongshan Ophthalmic Center, Sun Yat-sen University1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China54

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

05

Related compounds

06

Questions about Anrikefon trials

How many clinical trials are testing Anrikefon?

5 current trials in our China register name Anrikefon (also registered as HSK21542) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Anrikefon trials recruiting patients?

Yes. 4 of the 5 trials are recruiting: 4 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 Anrikefon clinical trials?

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School (1), Zhujiang Hospital (1), Affiliated Hospital of Guangdong Medical University (1) and Peking University First Hospital (1), among 5 lead sponsors in total. 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 Anrikefon works or whether it is effective, and it is not medical advice.

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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 Anrikefon 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 Anrikefon (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.