Study of Diphereline 3.75 mg Treatment In Women Suffering From Internal Genital Endometriosis
Launched by IPSEN · Jul 12, 2018
Trial Information
Current as of July 21, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Premenopausal women aged 25-40 years old
- • With symptomatic internal genital endometriosis - at least mild menorrhagia present or worse
- • Internal genital endometriosis diagnosis is based on enlarged uterus detected by pelvic bimanual examination and ultrasound examination (stages I-II-III by Demidov in accordance with ultrasound results not earlier than 2 months before first injection
- • Naive patients who have never been prescribed a GnRH agonist
- Exclusion Criteria:
- • Pregnant subjects
- • Subjects with hypersensitivity to GnRH analogue or to one of its excipients
- • Subjects treated with any other investigational drug within the last 30 days before study entry
- • Subjects' refusal to participate in the study
About Ipsen
Ipsen is a global biopharmaceutical group dedicated to innovation and specialty care, focusing on the discovery, development, and commercialization of transformative medicines for patients with serious diseases. With a strong emphasis on oncology, neuroscience, and rare diseases, Ipsen leverages cutting-edge research and advanced technologies to deliver high-quality therapies that address unmet medical needs. Committed to scientific excellence and ethical practices, Ipsen collaborates with healthcare professionals and stakeholders to drive patient-centered solutions and improve health outcomes worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Moscow, , Russian Federation
Balashikha, , Russian Federation
Irkutsk, , Russian Federation
Irkutsk, , Russian Federation
Kazan, , Russian Federation
Krasnodar, , Russian Federation
Krasnodar, , Russian Federation
Moscow, , Russian Federation
Moscow, , Russian Federation
Moscow, , Russian Federation
Moscow, , Russian Federation
Moscow, , Russian Federation
Nizhny Novgorod, , Russian Federation
Nizhny Novgorod, , Russian Federation
Novosibirsk, , Russian Federation
Novosibirsk, , Russian Federation
Novosibirsk, , Russian Federation
Odintsovo, , Russian Federation
Rostov On Don, , Russian Federation
Rostov On Don, , Russian Federation
Rostov On Don, , Russian Federation
Rostov On Don, , Russian Federation
Rostov On Don, , Russian Federation
Saint Petersburg, , Russian Federation
Saint Petersburg, , Russian Federation
Saint Petersburg, , Russian Federation
Samara, , Russian Federation
Saratov, , Russian Federation
Saratov, , Russian Federation
Saratov, , Russian Federation
Ufa, , Russian Federation
Volgograd, , Russian Federation
Yaroslavl, , Russian Federation
Yaroslavl, , Russian Federation
Patients applied
Trial Officials
Ipsen Study Director
Study Director
Ipsen
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials