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A Study Evaluating the Pharmacokinetics of Three QRL-101 Formulations in Healthy Participants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-518833-27-00
Acronym
QRL-101-06
Enrollment
24
Registered
2024-12-19
Start date
2025-01-10
Completion date
2025-05-15
Last updated
2025-05-28

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

Conditions

Amyotrophic Lateral Sclerosis (ALS)

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