Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**AD-102** is Addpharma's oral fixed-dose combination of raloxifene and cholecalciferol developed for postmenopausal osteoporosis. The product combines raloxifene, a selective estrogen receptor modulator that produces estrogenic effects in bone and reduces bone resorption, with cholecalciferol, a vitamin D3 prohormone that is converted to calcitriol and supports calcium and phosphate homeostasis through vitamin D receptor signaling. In the completed randomized crossover bioequivalence study NCT03824171, AD-102 was administered as raloxifene 45 mg plus cholecalciferol 800 IU tablets and compared with raloxifene 60 mg plus cholecalciferol 800 IU. Addpharma reported bioequivalence confirmation in 2020 and a marketing-authorization filing for postmenopausal osteoporosis in November 2020. ([ctv.veeva.com](https://ctv.veeva.com/study/evaluating-the-pharmacokinetic-characteristics-of-ad-102-in-healthy-volunteers))
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on AD-102.