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NCT07024316: ATL001-PII-CEP

A Study to Investigate the Improvement of Photosensitivity in Terms of Skin Lesions Associated With CEP Following Administration of Oral ATL-001 (Ciclopirox Oral Solution) in Participants Aged >18 Years of Age With CEP

Recruiting now Phase 1, PHASE2 Last updated 24 March 2026
What this trial tests

Phase 1, PHASE2 trial testing ATL-001 (Ciclopirox oral solution) in Congenital Erythropoietic Porphyria (CEP) in 6 participants. Currently enrolling.

Timeline
29 January 2026
Primary endpoint
1 May 2028
1 June 2028

Quick facts

Lead sponsorAtlas Molecular Pharma
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment6
Start date29 January 2026
Primary completion1 May 2028
Estimated completion1 June 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Atlas Molecular Pharma — full company profile →

Who can join

18 and older, any sex, with Congenital Erythropoietic Porphyria (CEP). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a study to investigate the effect of oral ATL-001 (ciclopirox) in CEP (Congenital Erythropoietic Porphyria) patients. During the study, it will be measured the improvement of skin lesions, fatigue and other clinical symptoms as well as blood parameters. Funding source - FDA OOPD

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Atlas Molecular Pharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07024316.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing