Shots:

• The BT designation is provided on three results from three XLHED subjects with a course of ER-004 intra-amniotic injections during the third trimester of pregnancy while the results were published in NEJM and showed profound and life-changing effects on infants
• The US FDA’s BT designation is granted to expedite the development and review of drugs for serious or life-threatening conditions allowing the program to benefit from all the FDA's fast-track program feature
• In H2’21- EspeRare to enroll patients for the study which is also benefited with Fast Track and ODD and has also received the EMA’s PRIME designation and ODD

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