Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Active, not recruiting Phase 1

A Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Doses of Prosetin in Healthy Volunteers and Participants With ALS

NCT05279755 · tracked via the Priya Life Science Netherlands tracker
Sponsor
ProJenX
Phase
Phase 1
Started
2022-02-26
Last updated
2026-04-27

Condition(s) studied

Amyotrophic Lateral Sclerosis

Investigational drug(s) / intervention(s)

prosetinplacebo

prosetin: oral solution

placebo: oral solution

Study summary

The primary purpose of this study is to evaluate the safety and tolerability of prosetin in healthy volunteers and participants with ALS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
PRO-101, Parts A and B, were completed in healthy volunteers. PRO-101, Parts C and D are ongoing in participants with ALS. Key eligibility criteria are summarized below: Key Inclusion Criteria - Part C * Adults ≥18 years of age * Diagnosis of ALS based on the Gold Coast diagnostic criteria * Slow Vital Capacity (SVC) \>50% predicted * If being concomitantly treated with riluzole and/or locally approved standard of care treatments, the participant must be on a stable dose for at least 30 days prior to screening and throughout the study * In the opinion of the Investigator, participant is able to swallow liquid in order to ingest the study medication. Key Exclusion Criteria - Part C * Active dementia, neurologic diseases other than ALS, or psychiatric illness that in the opinion of the investigator would affect participation in the current study. * Significant history or clinical manifestation of comorbid disease in any organ system that currently requires active treatment or is likely to require treatment during the study. * Any episodes of vertigo in the previous 12 months prior to screening. * Any medical history of seizures, or any clinically significant EEG finding at Screening or at Day -1. * A diagnosis of cancer or evidence of continued disease within five years before screening. Protocol-specified exceptions may be considered with approval from the Sponsor's Medical Monitor. * Participation in any other investigational study drug trial in which receipt of an investigational study drug occurred within 30 days prior to the first dose of study medication. * Prior exposure to any stem cell or gene therapies (investigational or off-label) for the treatment of ALS. Key Inclusion Criteria- Part D Participants who meet all of the following criteria may be included in Part D of the study: * Participants must have completed 14 days of blinded treatment in Part C. * Participants taking approved ALS standard-of-care medications must remain on stable doses through Day 28 of open-label treatment. * In the judgment of the Investigator, the participant's participation in the open-label portion of the study is medically appropriate Key Exclusion Criteria- Part D * Treatment with any other investigational drug or device throughout the duration of the study is excluded, with the exception of any COVID-19 vaccine or treatment with an emergency use authorization. NOTE: Other protocol-defined Inclusion/Exclusion Criteria may apply. Please contact trials@projenx.com with any questions about eligibility criteria.

Primary outcome measure(s)

  • Parts A, B, C, D: Number of Participants Experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs) — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, D: Number of Participants with Clinically Significant Laboratory Test Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, D: Number of Participants with Clinically Significant Vital Signs Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, and D: Number of Participants with Clinically Significant Electrocardiogram (ECG) Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, and D: Number of Participants with Clinically Significant Physical Examination Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, and D: Number of Participants with Clinically Significant Neurological Examination Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts A, B, C, and D: Number of Participants with Clinically Significant Ophthalmic Examination Abnormalities — Part A: Up to 28 days; Part B: Up to 42 days; Part C: Up to 28 days; Part D: Up to 54 weeks
  • Parts C and D: Number of Participants with Clinically Significant Electroencephalogram (EEG) Abnormalities — Part C: Up to 28 days; Part D: Up to 54 weeks

Trial sites (4)

FacilityCityRegionStatus
Massachusetts General Hospital Boston Massachusetts
Worldwide Clinical Trials Early Phase Services San Antonio Texas
The Neuro - Montréal Neurological Institute-Hospital Montreal Quebec
University Medical Center Utrecht Utrecht Utrecht
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05279755 on ClinicalTrials.gov ↗ ← All trials in the Netherlands