Roivant Sciences Ltd. Common Shares - ROIV STOCK NEWS

Roivant Sciences reported strong early demand for VTAMA, with 14,000 prescriptions in the first 11 weeks post-launch, marking it as the top prescribed topical for psoriasis in the US. The company announced a net loss of $353.8 million for Q1 2022, up from $101.1 million in Q1 2021. R&D expenses increased to $135.8 million, and SG&A expenses rose to $149.1 million, largely due to heightened share-based compensation. The ongoing trials for brepocitinib and tapinarof are progressing well, with data expected in late 2023. Investor day scheduled for September 28 will provide further updates.

Roivant Sciences (Nasdaq: ROIV) announced an investor call and webcast on August 15, 2022, at 8:00 a.m. EDT, to discuss its financial results for Q1 ended June 30, 2022, and provide a corporate update. Additionally, an investor day is scheduled for September 28, 2022, at 11:00 a.m. EDT, to offer updates on Roivant and its subsidiaries, known as Vants. The company aims to improve healthcare delivery and develop transformative medicines more efficiently. The press release serves as a reminder for both events, intended for investor engagement and transparency.

Roivant Sciences has reported significant developments and financial results for the fiscal year ending March 31, 2022. The FDA approved VTAMA (tapinarof) for plaque psoriasis, marking a milestone as the first new chemical entity in 25 years. With $2.1 billion in cash, Roivant prioritizes its pipeline and has initiated a strategic review, discontinuing non-essential programs to focus on high-value opportunities. Research and development expenses increased significantly, amounting to $483 million. Despite challenges, the company remains positioned for growth with ongoing trials and a robust commercial strategy.

Priovant Therapeutics, a collaboration between Roivant Sciences and Pfizer, is focusing on developing brepocitinib, a first-in-class dual inhibitor targeting TYK2 and JAK1. Earlier this quarter, a Phase 3 trial for dermatomyositis (VALOR) was initiated, while a Phase 2b study for systemic lupus erythematosus (SLE) is expected to yield results in the second half of 2023. Brepocitinib has shown statistically significant results in five prior placebo-controlled studies. The need for effective therapies in severe autoimmune diseases underscores the potential of brepocitinib in clinical treatments.

Roivant Sciences and Pfizer have launched Priovant Therapeutics to focus on developing innovative therapies for autoimmune diseases. Priovant is advancing brepocitinib, a dual inhibitor of TYK2 and JAK1, showing statistically significant results in five Phase 2 studies. A Phase 3 trial for dermatomyositis (VALOR) has commenced, and top-line results from an ongoing Phase 2b study in systemic lupus erythematosus (SLE) are expected in the second half of 2023. Pfizer retains a 25% equity stake in Priovant and has licensed rights for both brepocitinib and ropsacitinib.

Roivant Sciences (Nasdaq: ROIV) will host a live conference call and webcast on June 28, 2022, at 8:00 a.m. EDT to discuss its financial results for Q4 and the fiscal year ending March 31, 2022. Investors can join the call by dialing +1-844-224-1923 (domestic) or +1-214-989-7105 (international) using conference ID 1036178. A recording of the call will be available on Roivant’s website post-event. The company focuses on improving healthcare delivery and developing transformative medicines.

Dermavant Sciences announced the FDA's approval of VTAMA (tapinarof) cream, a steroid-free topical medication for plaque psoriasis in adults. In the pivotal Phase 3 trials, VTAMA cream showed significant efficacy, with 36%-40% of patients achieving clear skin compared to 6% with a vehicle. The remittive effect lasted approximately four months after treatment cessation. With a favorable safety profile and patient satisfaction rates over 80%, Dermavant aims for a June 2022 product launch. This positions VTAMA as a potential preferred treatment option in a market underserved by recent innovations.

Dermavant Sciences announced the FDA approval of VTAMA cream (tapinarof), a steroid-free treatment for plaque psoriasis in adults. The product showed significant efficacy in Phase 3 trials, with 36%-40% of patients achieving clear or almost clear skin at week 12. The cream provides a median off-treatment remittive effect of approximately four months. Dermavant plans to launch VTAMA in June 2022, with a fully staffed commercial team and manufacturing ready. This approval represents a milestone for Dermavant and offers a new option for patients with high unmet needs in psoriasis treatment.

Roivant Sciences (Nasdaq: ROIV) will participate in four upcoming healthcare investor conferences. CEO Matt Gline will present at the UBS Global Healthcare Conference on May 23, while CFO Richard Pulik will join a fireside chat at the H.C. Wainwright Conference on May 24. Gline will also participate in the Jefferies Healthcare Conference on June 8, followed by Pulik and President Mayukh Sukhatme at the Goldman Sachs Conference on June 14. Live webcasts of these events will be available on Roivant's investor website.