Roivant Sciences reported a net loss of $291.3 million for the quarter ended March 31, 2022. The company had $2.1 billion in cash and cash equivalents as of March 31, 2022. VTAMA was approved by the FDA for the treatment of plaque psoriasis.
VTAMA approved by FDA for the treatment of plaque psoriasis.
Priovant established in partnership with Pfizer to develop brepocitinib for autoimmune diseases.
Roivant reported $2.1B in cash and cash equivalents.
Early discovery efforts validated with multiple collaborations.
Roivant expects to provide updates on the commercial launch of VTAMA for psoriasis and report topline data from the Phase 3 clinical trials of VTAMA for the treatment of atopic dermatitis in the first half of calendar year 2023.