SYF124052c7b7e146aa9b8a24b0f3e5e8e3

Not Yet RecruitingPhase 1

Evaluation of the bioequivalence of two intravaginal gel pre...

CCDRD Cooperative Clinical Drug Research and Development AG Source

CTIS (EMA)

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Study Type

interventional

Reported enrollment (type unavailable)

N/A

Locations

1 country

Sites

2

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: not yet recruiting
Reported enrollment (type unavailable): Not reported
Study completion date: Not reported
Date not reported
Listed locations: 1 countries · 2 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
June 16, 2026
Actual (reported)

Conditions

No therapeutic indication in the current trial with healthy volunteers.

Sponsors & Collaborators

CCDRD Cooperative Clinical Drug Research and Development AG
Industrylead
Ioulia And Irene Tseti Pharmaceutical Laboratories S.A.
Industryco_sponsor

Study Sites (2)

Diagnostic Consultative Centre Ascendent EOOD

Sofia, 1202, Bulgaria

Ivo Bogdanov+35929839494 ivoatbog@gmail.com

Medical Center Neovitro OOD

Sofia, 1404, Bulgaria

Andrey Dimitrov Petrov+359875356300 andrewpbg@yahoo.com

Central Study Contacts

Project Manager

+49334223790 aseliger@ccdrdag.com

Head of RA

+302108072512

Study Design

Study Type: interventional
Phase: phase 1

Study Record Dates

First Submitted

June 16, 2026

Source record

Download the complete CTIS (EMA) record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: European Medicines Agency (EMA), Clinical Trials Information System (CTIS). Original record and public documents are available on CTIS.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: 2025-520498-38-00
Data provider: European Medicines Agency (EMA)
Normalization version: ctis-v1

Open registry record

Source retrieved: 2026-10-30 06:10:08 UTC

Locations

BG(2)

SYFca71c33bc66d4ea1855dc692f88042a9

Evaluation of the bioequivalence of two products containing esomeprazole under fasting conditions: Esomeprazole-Syrup 40 mg dose (Test) vs. Nexium 40 mg (Comparator). An open, randomized, single dose, four-period, replicate, crossover trial in healthy volunteers

Phase 1Unknown

SYF6ed0f8284d8b4f8889b4688057dd752f

Evaluation of bioequivalence of two products containing 400 mg ibuprofen and 100 mg caffeine: Ibuprofen / Caffeine 400 mg / 100 mg coated granules (Test) vs. Thomapyrin TENSION DUO, 400mg / 100mg Filmtabletten (Reference). A monocentric, open, randomized, single dose, two-period, crossover trial in healthy volunteers

Phase 1Unknown

SYF18720e83653e4c419f10d58646cac84c

Evaluation of the bioequivalence of two products containing esomeprazole under fed conditions: Esomeprazole-Syrup 40 mg dose (Test) vs. Nexium 40 mg (Comparator). An open, randomized, single dose, four-period, replicate, crossover trial in healthy volunteers

Phase 1Unknown

SYFce2256bb647d434da75c12fe9d8f48b2

Evaluation of bioequivalence of two products containing 600 mg ibuprofen: Ibuprofen Sopharma 600 mg film-coated tablets (Test) vs. Brufen 600 mg film-coated tablets (Comparator). A monocentric, open, randomized, single dose, two-period, crossover trial in healthy volunteers

Phase 1Unknown

SYF03e47ecc0eba45f9bc594971b02e04de

Single dose oral bioequivalence study of Cladribine 10 mg Tablets and Mavenclad® 10 mg tablets (Cladribine) in healthy adult human subjects under fed conditions

Phase 1Unknown

SYFb3b818a7a6ea4efa84f41d5e26a7cd29

Evaluation of the bioavailability of two products containing esomeprazole under fasting and fed conditions: Esomeprazole-Syrup 40 mg dose (Test) vs. Nexium 40 mg (Comparator). A monocentric, open, randomized, single dose, four-period, crossover trial in healthy volunteers

Phase 1Unknown

SYFf9c36b22e9754f51968fa19506e99f36

A study to investigate the similarity of two different Tiotropium inhalers in healthy volunteers.

Phase 1Unknown

soumelas@uni-pharma.gr