Condition: Contraception · Change in Bone Mineral Density · Sponsor: Insud Pharma
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.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Alabama Clinical Therapeutics, LLC | Alabaster, Alabama, United States | — |
| Alabama Clinical Therapeutics, LLC | Birmingham, Alabama, United States | — |
| Del Sol Research Management | Tucson, Arizona, United States | — |
| Eclipse Clinical Research | Tucson, Arizona, United States | — |
| Cornerstone Research Institute - Longwood | Altamonte Springs, Florida, United States | — |
| Encore Medical Research of Boynton Beach LLC. | Boynton Beach, Florida, United States | — |
| Women's Medical Research Group | Clearwater, Florida, United States | — |
| Direct Helpers Research Center | Hialeah, Florida, United States | — |
| Inpatient Research Clinic, LLC | Hialeah, Florida, United States | — |
| Vital Pharma Research, Inc. | Hialeah, Florida, United States | — |
| Encore Medical Research, LLC | Hollywood, Florida, United States | — |
| Global Research Associates | Homestead, Florida, United States | — |
+ 35 more locations — full list on the registry record.
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