Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Human placental hydrolysate is a standardized, pharmaceutical-grade biological preparation derived from healthy human donor placentas. It is produced through enzymatic hydrolysis (typically using pepsin and hydrochloric acid) followed by rigorous sterilization and filtration processes to ensure safety and eliminate viral or bacterial pathogens. The resulting extract is a complex, chemically heterogeneous mixture containing low-molecular-weight peptides, amino acids, nucleotides, vitamins, minerals, and trace growth factors such as hepatocyte growth factor (HGF) and insulin-like growth factor 1 (IGF-1). It is widely utilized in East Asia and Russia for its hepatoprotective, immunomodulatory, anti-inflammatory, and tissue-regenerative properties. Standardized formulations are marketed under several brand names, including Laennec (approved for improving liver function in chronic liver disease) and Melsmon (approved for menopausal disorders and milk secretion deficiency). Additionally, it is investigated for various off-label and clinical-stage indications, including chronic fatigue syndrome, musculoskeletal pain, and neurodegenerative conditions such as multiple sclerosis.
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 human placental hydrolysate.