Skip to content

A Study Evaluating the Safety and Tolerability of a Novel Formulation of QRL-101 in Healthy Participants

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524310-28-00
Acronym
QRL-101-08
Enrollment
48
Registered
2026-01-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

amotrophic lateral sclerosis, Epilepsy, neuropathy

Interventions

None listed

Sponsors

Quralis Corp.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Netherlands

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026