A randomized, investigator masked pilot study to establish the experimental conditions and select the criteria to compare topical application of 2 methyl aminolevulinate creams: evaluation of protoporphyrin IX formation in the skin of healthy subjects.

2023-504881-42-01 Protocol TOP009 Human pharmacology (Phase I) - Other Ended

Start 25 Sep 2024 · End 18 Oct 2024 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol TOP009

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 12
Countries 1
Sites 1

None - Healthy subjects

Key facts

Sponsor
Substipharm
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
25 Sep 2024 → 18 Oct 2024
Decision date (initial)
2024-07-25
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

None - Healthy subjects

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Substipharm

Sponsor organisation
Substipharm
Address
24 Rue Erlanger
City
Paris
Postcode
75016
Country
France

Scientific contact point

Organisation
Substipharm
Contact name
Janusz Czernielewski

Public contact point

Organisation
Substipharm
Contact name
Janusz Czernielewski

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
France Ended 12 1
Rest of world 0

Investigational sites

France

1 site · Ended
Centre De Pharmacologie Clinique Appliquee A La Dermatologie
CPCAD, 151 Route De Saint Antoine, 06200, Nice

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
France 2024-09-25 2024-10-18 2024-09-25 2024-10-18

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-04-11 France Acceptable
2024-07-25
2024-07-25