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A single-centre, open-label, randomised, phase II study on the maintenance of ovulation inhibition after intentional application errors during 84 days of treatment with MR-130A-01 contraceptive transdermal patch

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522565-30-00
Acronym
MR-130A-01-TD-2002
Enrollment
60
Registered
2025-11-17
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Investigation of maintenance of ovulation inhibition after intentional application errors for indication of contraception in healthy subjects

Brief summary

Ovulation incidence in cycles with regular application, in cycles with 24h application errors & in cycles with 48h application errors. Ovulation is defined as Hoogland-Skouby score 5 or 6 in combination with positive Landgren criterion (i.e., rupture, or development into a luteinized unruptured follicle, of a follicle like structure > 13 mm, with concomitant estradiol [E2] concentrations >100 pmol/L & followed by a luteal phase with progesterone [P] concentrations > 16.0 nmol/L during ≥ 5 days

Detailed description

• Ovulation incidence overall • Ovulation incidence per treatment cycle, HSS determined for each treatment cycle, Fulfilment of Landgren criterion in cycles with HSS 5 or 6, FLS diameter and endometrial thickness determined by Transvaginal Ultrasonography (TVUS), Pituitary (luteinizing hormone [LH]) and ovarian (estradiol [E2], progesterone [P]) hormone concentrations in serum, Plasma concentration of NGMN and its metabolite norgestrel determined: immediately (5min) before and at the end of one scheduled patch-free window (once each per 24/48-hour application-error cycle), and immediately (5min) before application of a new patch (trough, once per regular-application cycle), Plasma concentrations of NGMN and norgestrel, Assessment of adhesion score by the participants themselves and by the site personnel, Safety and tolerability: treatment-emergent Adverse Events (TEAE); safety clinical laboratory parameters; incidence of application site reactions (skin irritation scores assessed by the participants), Bleeding pattern determined as incidences of bleeding and/or spotting episodes, number of observed days of bleeding and/or spotting, bleeding only and spotting only, incidences of complete absence of bleeding or spotting (excluding the first episode)

Interventions

DRUGMR-130A-01

Sponsors

Mylan Pharmaceuticals Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Ovulation incidence in cycles with regular application, in cycles with 24h application errors & in cycles with 48h application errors. Ovulation is defined as Hoogland-Skouby score 5 or 6 in combination with positive Landgren criterion (i.e., rupture, or development into a luteinized unruptured follicle, of a follicle like structure > 13 mm, with concomitant estradiol [E2] concentrations >100 pmol/L & followed by a luteal phase with progesterone [P] concentrations > 16.0 nmol/L during ≥ 5 days

Secondary

MeasureTime frame
• Ovulation incidence overall • Ovulation incidence per treatment cycle, HSS determined for each treatment cycle, Fulfilment of Landgren criterion in cycles with HSS 5 or 6, FLS diameter and endometrial thickness determined by Transvaginal Ultrasonography (TVUS), Pituitary (luteinizing hormone [LH]) and ovarian (estradiol [E2], progesterone [P]) hormone concentrations in serum, Plasma concentration of NGMN and its metabolite norgestrel determined: immediately (5min) before and at the end of one scheduled patch-free window (once each per 24/48-hour application-error cycle), and immediately (5min) before application of a new patch (trough, once per regular-application cycle), Plasma concentrations of NGMN and norgestrel, Assessment of adhesion score by the participants themselves and by the site personnel, Safety and tolerability: treatment-emergent Adverse Events (TEAE); safety clinical laboratory parameters; incidence of application site reactions (skin irritation scores assessed by th

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026