Ignite Creation Date:
2025-12-24 @ 10:20 PM
Ignite Modification Date:
2026-01-01 @ 12:07 PM
Study NCT ID:
NCT06867835
Status:
RECRUITING
Last Update Posted:
2025-07-14
First Post:
2025-02-19
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'C476721', 'term': 'bremelanotide'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 10}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2025-06-26', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-07', 'completionDateStruct': {'date': '2025-12', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-07-09', 'studyFirstSubmitDate': '2025-02-19', 'studyFirstSubmitQcDate': '2025-03-05', 'lastUpdatePostDateStruct': {'date': '2025-07-14', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2025-03-10', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-09', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Levels of Bremelanotide (BMT) in Breast Milk Over 24h After Administration of Vyleesi', 'timeFrame': '24 hours', 'description': 'The levels/concentrations of bremelanotide (BMT) will be measured in breast milk samples collected at different timepoints up to 24h from lactating women who receive a single dose of Vyleesi (BMT 1.75 mg SC).'}, {'measure': 'Area under the curve from time 0 to end of dosing interval (AUCtau) for BMT in Breast Milk', 'timeFrame': '24 hours'}, {'measure': 'Maximum observed concentration (Cmax) of BMT in breast milk', 'timeFrame': '24 hours'}, {'measure': 'Time to reach Cmax of BMT in breast milk (Tmax)', 'timeFrame': '24 hours'}, {'measure': 'Terminal half-life of BMT in breast milk (t1/2)', 'timeFrame': '24 hours'}], 'secondaryOutcomes': [{'measure': 'Levels of Bremelanotide (BMT) in Plasma Over 24h After Administration of Vyleesi', 'timeFrame': '24 hours'}, {'measure': 'Area under the curve from time 0 to end of dosing interval (AUCtau) for BMT in Plasma', 'timeFrame': '24 hours'}, {'measure': 'Maximum observed concentration (Cmax) of BMT in Plasma', 'timeFrame': '24 hours'}, {'measure': 'Time to reach Cmax of BMT in Plasma (Tmax)', 'timeFrame': '24 hours'}, {'measure': 'Milk:plasma ratio (M/P) of BMT Levels', 'timeFrame': '24 hours'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': False, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Lactating Mother']}, 'descriptionModule': {'briefSummary': 'The primary objectives of this clinical trial performed with Vyleesi (Bremelanotide Injection) are:\n\n* to evaluate if Bremelanotide (BMT) is secreted in breast milk of lactating women treated with a single dose of BMT 1.75 mg SC.\n* to measure the concentration and characterize the pharmacokinetics of BMT secreted in breast milk of lactating women treated with a single dose of BMT 1.75 mg SC.\n\nThis open-label, pharmacokinetic (PK) study will be performed in 10 healthy lactating female subjects between 10 days and 6 months post-partum (inclusive). The maximum duration of subject participation in the study will be approximately 29 days, consisting of 3-week Screening period, a 1 day treatment period, and up to a 7 day follow-up period.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT'], 'maximumAge': '55 Years', 'minimumAge': '18 Years', 'genderBased': True, 'genderDescription': 'Lactating mother', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria (Main Criteria):\n\n* Female subjects ≥18 to 55 years of age (inclusive) and premenopausal\n* Lactating, between 10 days and 6 months postpartum (inclusive).\n* Exclusively breastfeeds their infant prior to participation in the study\n* Is willing to pump and store breastmilk for feeding her infant for a minimum of 48 hours in advance of study initiation and discontinue breastfeeding their infant for the duration of their study participation (beginning from time of dosing with BMT) and a minimum of 24 hours following the Safety Follow-Up visit (i.e., a minimum of 48 hours following dosing with BMT).\n* Ensure at the time of screening that the breastfed infant can feed from a bottle during maternal participation in the study\n* The subject is not pregnant, and does not intend to become pregnant before, during, or within 1 complete menstrual cycle or 2 months after administration of study drug\n* Subjects of childbearing potential who are sexually active with a nonsterilized male partner must have stable, continuous use of an acceptable method of contraception throughout the duration of the study, and for at least 60 days after the dose of study drug\n\nExclusion Criteria (Main Criteria):\n\n* Breastfeeding is not well established in the mother-infant pair (e.g., poor latching of the infant or low milk supply).\n* Any condition that interferes with the successful collection of milk from one or both breasts including but not limited to lactation mastitis (typically presents as a tender, hot, swollen area of the breast that may or may not involve an infection), milk blister that may present as a blocked nipple pore, breast abscess, etc.\n* Has used any investigational compound and/or an experimental medical device within 28 days before Screening.\n* Has taken BMT within 24 hours of participation in the study'}, 'identificationModule': {'nctId': 'NCT06867835', 'briefTitle': 'Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk', 'organization': {'class': 'INDUSTRY', 'fullName': 'Cosette Pharmaceuticals, Inc.'}, 'officialTitle': 'A Phase 4, Open-Label Study of a Single Dose of Vyleesi® (Bremelanotide Injection) in Healthy, Premenopausal Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast Milk', 'orgStudyIdInfo': {'id': 'PMR 3635-3'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Vyleesi', 'description': 'One dose of BMT 1.75 mg SC on Day 1', 'interventionNames': ['Drug: Vyleesi (Bremelanotide Injection)']}], 'interventions': [{'name': 'Vyleesi (Bremelanotide Injection)', 'type': 'DRUG', 'description': 'Single dose of BMT 1.75 mg SC on Day 1', 'armGroupLabels': ['Vyleesi']}]}, 'contactsLocationsModule': {'locations': [{'zip': '33178', 'city': 'Doral', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'First Excellence Research Group LLC', 'geoPoint': {'lat': 25.81954, 'lon': -80.35533}}], 'centralContacts': [{'name': 'CRA', 'role': 'CONTACT', 'email': 'vishnu.kambham@cbcc.global', 'phone': '+1 (203)-895 2242'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Cosette Pharmaceuticals, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}