Drugs / QRL-101
last change Aug 2026 re-read 3 minutes ago

QRL-101

Developed for
amyotrophic lateral sclerosis
Investigated by
QurAlis Corporation · Centre for Human Drug Research, Netherlands

Trials 6

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07421778 Feb → Aug 2026 overdue — QurAlis Corporation Recruiting No outcome recorded
Phase 1 NCT06877624 Jan → May 2025 — QurAlis Corporation Completed No outcome recorded
Phase 1 NCT06714396 Nov 2024 → Aug 2025 amyotrophic lateral sclerosis QurAlis Corporation Completed No outcome recorded
Phase 1 NCT06681441 Oct → Dec 2024 — QurAlis Corporation Completed No outcome recorded
Phase 1 NCT06532396 Jul → Dec 2024 — QurAlis Corporation Completed No outcome recorded
Phase 1 NCT05667779 Dec 2022 → Dec 2023 — QurAlis Corporation Completed No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2025-12-29 QurAlis Corporation Results QurAlis Confirms Signal of Target Engagement in ALS Patients in Phase 1 Clinical Trial of QRL-101, a Potentially Best-in-Class Selective Kv7.2/7.3 Ion Channel Opener quralis.com ↗
QurAlis Corporation (“QurAlis”), a clinical-stage biotechnology company driving scientific breakthroughs into powerful precision medicines that have the potential to alter the trajectory of neurodegenerative and neurological diseases, today announced topline data from its Phase 1 proof-of-mechanism (PoM) clinical trial of QRL-101 in people living with amyotrophic lateral sclerosis (ALS).
2025-12-02 QurAlis Corporation Results QurAlis to Present Data From its Phase 1 Clinical Trial of QRL-101, a Potential Best-in-Class Selective Kv7.2/7.3 Ion Channel Opener, at American Epilepsy Society 2025 Annual Meeting quralis.com ↗
The study shows evidence of brain penetration, target engagement, and potential anti-seizure effects demonstrated through biomarkers for transcranial magnetic stimulation electromyography (TMS-EMG) and electroencephalography (EEG).
2025-03-12 QurAlis Corporation Results QurAlis Announces Topline Data From its Phase 1 Clinical Trial of QRL-101 Evaluating Biomarkers of ALS and Epilepsy in Healthy Volunteers quralis.com ↗
Topline results demonstrated a dose-dependent, statistically significant decrease in motor nerve excitability threshold tracking (mNETT) strength-duration time constant (SDTC), the co-primary endpoint of the trial related to ALS.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as QRL-101 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06877624 ↗
5

NCT05667779 ↗

NCT07421778 ↗

NCT06714396 ↗

NCT06681441 ↗

NCT06532396 ↗

Route Oral “Single-ascending doses of QRL-101 will be orally administered.” NCT05667779 ↗