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Compound · clinical trials

EA5

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name EA5 as an intervention. Synced 25 Sep 2026
2Trials tracked
1Recruiting now
1Lead sponsor
1Country register
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

EA5 is named as a drug or biological intervention in 2 clinical trials in our China trial register, 1 of which is recruiting. The lead sponsor is Shanghai Lanyi Therapeutics Co., Ltd.. Registered phase: Phase 1. Conditions studied include PNH - Paroxysmal Nocturnal Hemoglobinuria; Generalized Myasthenia Gravis (gMG).

01

Clinical trials of EA5

2 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT07256301 A Phase Ib, Multicenter, Open-Label Study of Multiple-Dose EA5 in Adults With Paroxysmal Nocturnal Hemoglobinuria (PNH) (ClinicalTrials.gov ↗)
PNH - Paroxysmal Nocturnal Hemoglobinuria
Phase 1 Recruiting Shanghai Lanyi Therapeutics Co., Ltd. China
NCT07818291 An Open-label, Dose-escalation Phase Ib Study of EA5 Injection in Adults With Anti-AChR Antibody-Positive Generalized Myasthenia Gravis (ClinicalTrials.gov ↗)
Generalized Myasthenia Gravis (gMG)
Phase 1 Not yet open Shanghai Lanyi Therapeutics 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

2 conditions
Condition (as registered)Trials
PNH - Paroxysmal Nocturnal Hemoglobinuria1
Generalized Myasthenia Gravis (gMG)1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Shanghai Lanyi Therapeutics Co., Ltd.2
04

Trials by country register

RegisterEA5 trials
Clinical trials in China2

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

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how EA5 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 EA5 (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 25 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 โ€” 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 โ€” we correct promptly and log it.