Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Misotac is a pharmaceutical product containing misoprostol, a synthetic analogue of prostaglandin E1 (PGE1). Produced by Sigma Pharmaceutical Industries in Egypt, it is typically formulated as 200 microgram tablets for oral, sublingual, vaginal, or rectal administration. The drug is extensively utilized in obstetrics and gynecology for its potent uterotonic and cervical-ripening properties. Its primary mechanism of action involves acting as an agonist at prostaglandin receptors in the uterine myometrium, leading to increased strength and frequency of contractions, and in the cervix, where it promotes collagen degradation and softening. Clinically, Misotac is employed for medical abortion, induction of labor, the prevention and treatment of postpartum hemorrhage (particularly during cesarean sections), and cervical priming prior to diagnostic or surgical procedures. It is also being investigated for reducing blood loss in surgeries such as myomectomies and treating abnormal uterine bleeding associated with isthmocele. Misotac's stability at room temperature and ease of administration make it a critical therapeutic option in various clinical settings.
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 Misotac.