Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
QueeZy ER is an oral, extended-release fixed-dose combination drug developed and marketed by Jagsonpal Pharmaceuticals for the treatment of nausea and vomiting in pregnancy (NVP), commonly referred to as morning sickness. The formulation contains 20 mg of doxylamine succinate, an H1-antihistamine that blocks histamine receptors to alleviate nausea, and 20 mg of pyridoxine hydrochloride (Vitamin B6), which addresses nutritional deficiencies associated with pregnancy-related emesis. Utilizing a specialized tablet-in-tablet technology, QueeZy ER provides a dual-release profile that offers both immediate and prolonged symptom relief over a 24-hour period. This extended-release formulation is designed to improve patient compliance by reducing the dosing frequency to a single daily tablet, compared to conventional multi-dose regimens. It is approved and launched in India for pregnant women experiencing morning sickness and related symptoms.
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 QueeZy ER.