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A PHASE 1B, MULTICENTER, RANDOMIZED, PLACEBO- CONTROLLED, DOUBLE-BLIND STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND BIOLOGICAL ACTIVITY OF TQS-168 IN SUBJECTS WITH AMYOTROPHIC LATERAL SCLEROSIS

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-504746-54-00
Acronym
TQS-168-ALS-101
Enrollment
16
Registered
2023-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-11

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

Conditions

AMYOTROPHIC LATERAL SCLEROSIS

Interventions

None listed

Sponsors

Tranquis Therapeutics Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Latvia

Outcome results

None listed

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