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Search / Trial NCT03586063

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.

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

0 patients applied

Trial Officials

Ipsen Study Director

Study Director

Ipsen

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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