CDSCO Panel Tells Abbott India to revise phase IV CT protocol of Dydrogesterone plus Estradiol Tablets
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organization (CDSCO) has opined the drug major Abbott India to revise the Phase IV clinical trial protocol of the fixed-dose combination (FDC) of Dydrogesterone plus Estradiol in accordance with In inclusion criteria, primary endpoint, secondary endpoint.
In addition, the expert panel stated that the objective criteria need to be defined for mild, moderate, and severe hot flashes depending on quality of life (QOL) scale scoring.
This came after Abbott India presented the revised Phase IV clinical trial protocol of Dydrogesterone plus Estradiol ( 2.5 mg plus 0.5mg) tablets before the committee.
Dydrogesterone is a synthetic progestogen that works similarly to progesterone (female hormone). It is used to treat menstrual disorders caused by a lack of hormones in women. It's also used to help prevent miscarriages and abortions. The drug is used mainly to relieve pain and menstrual cramps.
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