Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

HS235 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA, UK and Spain registers that name HS235 as an intervention. Synced 9 Nov 2026
2Current trials
2Recruiting now
1Lead sponsor
3Country registers
At a glance

HS235 is named as an intervention in 2 current clinical trials in our USA, UK and Spain registers. 2 are recruiting patients now. All registered phases are Phase 1/2. The lead sponsor is 35Pharma Inc., a GSK company. The most-studied condition is Pulmonary Arterial Hypertension.

Patient leaflets for HS235

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

  • Recruiting2100%

Trials by phase

  • Phase 1/22100%
01

Clinical trials of HS235

2 trials
StudyPhaseStatusLead sponsorRegisters
HS235 Study in Overweight and Obese Participants With Combined Pre and Post-Capillary Pulmonary Hypertension Due to Heart Failure With Preserved Ejection Fraction
NCT07123779 · Pulmonary Hypertension, Heart Failure With Preserved Ejection Fraction
Phase 1/2 Recruiting 35Pharma Inc., a GSK company USA
A Study of HS235 for Treatment of Pulmonary Arterial Hypertension (PAH) in Adults
NCT07143448 · Pulmonary Arterial Hypertension
Phase 1/2 Recruiting 35Pharma Inc., a GSK company UK, USA, Spain

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 HS235

3 conditions
Pulmonary Arterial Hypertension1Pulmonary Hypertension1Heart Failure With Preserved Ejection Fraction1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
35Pharma Inc., a GSK company2
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA22
Clinical trials in UK11
Clinical trials in Spain11

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

05

Related compounds

06

Questions about HS235 trials

How many clinical trials are testing HS235?

2 current trials in our USA, UK and Spain registers name HS235 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are HS235 trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 2 with sites in USA, 1 with sites in UK and 1 with sites in Spain. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors HS235 clinical trials?

The lead sponsor is 35Pharma Inc., a GSK company. 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 HS235 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 HS235 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 HS235 (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 9 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.