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NCT07371338

Phase 1 Clinical Trial to Evaluate the Safety, Efficacy, and Pharmacokinetics of IPS101A in Parkinson's Disease Patients

Recruiting now Phase 1 Last updated 25 March 2026
What this trial tests

Phase 1 trial testing IPS101A in Parkinson Disease in 6 participants. Currently enrolling.

Timeline
30 May 2026
Primary endpoint
31 October 2027
31 December 2027

Quick facts

Lead sponsorInnopeutics Corporation
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment6
Start date30 May 2026
Primary completion31 October 2027
Estimated completion31 December 2027
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Innopeutics Corporation — full company profile →

Who can join

Adults 50 to 80, any sex, with Parkinson Disease or Parkinson's Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the dose-related safety and tolerability of IPS101A, an adeno-associated virus (AAV) gene therapy, in patients with Parkinson's disease who exhibit severe functional impairment corresponding to Hoehn \& Yahr stages 4-5 and whose symptoms are not adequately controlled despite all available monotherapy and combination therapy options. In addition, the study aims to assess the maximum tolerated dose (MTD) of IPS101A, as well as its preliminary efficacy and pharmacokinetic (PK) characteristics.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Parkinson Disease

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07371338.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing