Bioequivalence of Lisdexamfetamine dimesylate 20 mg Capsules in Healthy Participants Under Fasting Conditions.

2024-516827-14-00 Protocol BLCL-LIS-EU-02 Human pharmacology (Phase I) - Bioequivalence study Ended

Start 10 Mar 2025 · End 15 Apr 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol BLCL-LIS-EU-02

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Bioequivalence study
Status Ended
Participants planned 24
Countries 1
Sites 1

No medical condition.

Key facts

Sponsor
Pharmaplot P.C.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
10 Mar 2025 → 15 Apr 2025
Decision date (initial)
2024-10-02
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

No medical condition.

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Pharmaplot P.C.

Sponsor organisation
Pharmaplot P.C.
Address
Kleisthenous And 40a Mouson St
City
Athens
Postcode
153 44
Country
Greece

Scientific contact point

Organisation
Pharmaplot P.C.
Contact name
PharmaPlot PC, Regulatory Affairs Department

Public contact point

Organisation
Pharmaplot P.C.
Contact name
PharmaPlot PC, Regulatory Affairs Department

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Portugal Ended 24 1
Rest of world 0

Investigational sites

Portugal

1 site · Ended
Blueclinical Investigacao E Desenvolvimento Em Saude Lda.
Medical Management, Rua De Sarmento De Beires 153 0 Floor 3rd Floor, 4250-449, Porto

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Portugal 2025-03-10 2025-04-15 2025-03-10 2025-04-01

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-08-16 Portugal Acceptable
2024-09-20
2024-10-02
2 NON SUBSTANTIAL MODIFICATION NSM-1 2025-02-27 Portugal Acceptable
2024-09-20
2025-02-27
3 SUBSTANTIAL MODIFICATION SM-1 2025-02-27 Portugal Acceptable
2025-03-25
2025-03-25