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Study identifier: NCT05461573 Synced from ClinicalTrials.gov · August 04, 2026
● Completed

Efficacy, Safety, and Tolerability of LPRI-CF113 as an Oral Contraceptive in Females

Condition: Contraception · Change in Bone Mineral Density  ·  Sponsor: Insud Pharma

PhasePhase 3
Planned participants1542
Who can joinFemale, 13 Years to 45 Years
Healthy volunteersYes

About this study

This study will be in two parts, Part A and Part B. The primary objective of Part A is to evaluate the contraceptive efficacy of LPRI-CF113. The secondary objective of Part A is to evaluate the safety and tolerability of LPRI-CF113. The primary objective of Part B is to evaluate the impact of LPRI-CF113 on bone mineral density (BMD) at the lumbar spine (L1-L4) after 12 months (13 medication cycles). The secondary objective of Part B is to evaluate the impact of LPRI-CF113 on BMD and bone turnover after 12 months (13 medication cycles) at the femoral neck, total hip, and total body.

This description comes directly from the study's public registry record.

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No contact information is available for this study as per the public registry record.

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Locations (47)

Alabama Clinical Therapeutics, LLCAlabaster, Alabama, United States
Alabama Clinical Therapeutics, LLCBirmingham, Alabama, United States
Del Sol Research ManagementTucson, Arizona, United States
Eclipse Clinical ResearchTucson, Arizona, United States
Cornerstone Research Institute - LongwoodAltamonte Springs, Florida, United States
Encore Medical Research of Boynton Beach LLC.Boynton Beach, Florida, United States
Women's Medical Research GroupClearwater, Florida, United States
Direct Helpers Research CenterHialeah, Florida, United States
Inpatient Research Clinic, LLCHialeah, Florida, United States
Vital Pharma Research, Inc.Hialeah, Florida, United States
Encore Medical Research, LLCHollywood, Florida, United States
Global Research AssociatesHomestead, Florida, United States

+ 35 more locations — full list on the registry record.

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