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Phase I Trial: Quotient Code QSC300787

Phase I Trial: Quotient Code QSC300787

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14891667
Enrollment
84
Registered
2024-07-03
Start date
2024-07-10
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Healthy volunteers Not Applicable

Interventions

The Sponsor has confirmed that the trial meets the criteria for deferral of publication of the full details of the study. The full details will be added to the study records within 30 months after the

Sponsors

Alumis Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The Sponsor has confirmed that the trial meets the criteria for deferral of publication of the full details of the study. The full details will be added to the study records within 30 months after the trial has ended.

Exclusion criteria

Exclusion criteria: The Sponsor has confirmed that the trial meets the criteria for deferral of publication of the full details of the study. The full details will be added to the study records within 30 months after the trial has ended.

Design outcomes

Primary

MeasureTime frame
The Sponsor has confirmed that the trial meets the criteria for deferral of publication of the full details of the study. The full details will be added to the study records within 30 months after the trial has ended.

Secondary

MeasureTime frame
The Sponsor has confirmed that the trial meets the criteria for deferral of publication of the full details of the study. The full details will be added to the study records within 30 months after the trial has ended.

Countries

England, United Kingdom

Contacts

Public ContactClinical Trial Information Desk
info@alumis.com+1 (0)650 231 6625

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026