Welcome to our dedicated page for roivw news (Ticker: roivw), a resource for investors and traders seeking the latest updates and insights on roivw stock.
Riovant Sciences Ltd. is a commercial-stage biopharmaceutical company focused on accelerating the development and commercialization of medicines that matter. The company's pipeline includes VTAMA®, a topical treatment for psoriasis and atopic dermatitis, IMVT-1402 and batoclimab, fully human monoclonal antibodies targeting the neonatal Fc receptor in autoimmune indications, and brepocitinib, a small molecule inhibitor for dermatomyositis and non-infectious uveitis. Through creating nimble subsidiaries, Roivant aims to advance its therapies and technologies, while also nurturing discovery-stage companies and health tech startups.
Roivant Sciences announced the pricing of a public offering of 30 million common shares at $5.00 each, generating gross proceeds of $150 million. Roivant will receive approximately $100 million from the offering, while selling shareholders will obtain about $50 million. The underwriter has a 30-day option for an additional $22.5 million in shares. The offering is set to close on November 10, 2022, subject to conditions. Roivant expects its cash flow to sustain operations into the second half of 2025.
Roivant Sciences announced a proposed underwritten public offering of $150 million of common shares, with a 30-day option for the underwriter to purchase an additional $22.5 million. The offering is subject to market conditions, with no assurance on its completion or terms. Cantor Fitzgerald & Co. is the sole bookrunner for this offering. A registration statement for these securities was declared effective on October 3, 2022, and a preliminary prospectus supplement has been filed with the SEC. This announcement does not constitute an offer to sell securities.
Roivant Sciences (Nasdaq: ROIV) will host a conference call on November 14, 2022, at 8:00 a.m. EST to discuss its financial results for Q2 ended September 30, 2022, alongside a corporate update. The company is also participating in several investor conferences in November, including the Credit Suisse Annual Healthcare Conference and Jefferies London Healthcare Conference. Presentations by CFO Richard Pulik and CEO Matt Gline will provide insights on Roivant's strategic initiatives and outlook. Archived webcasts will be accessible on Roivant's investor website post-event.
Roivant Sciences (Nasdaq: ROIV) will participate in three healthcare investor conferences this September in Boston, New York, and London. The schedule includes:
- Citi BioPharma Conference in Boston on September 7
- H.C. Wainwright Global Investment Conference in New York on September 12, with CEO Matt Gline presenting at 8:30 a.m. EDT
- Bank of America Global Healthcare Conference in London on September 16
Additionally, Roivant will host a virtual Investor Day on September 28 at 11:00 a.m. EDT.
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 (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.
FAQ
What is Roivant Sciences Ltd. focused on?
What are some products in Roivant Sciences Ltd.'s pipeline?
How does Roivant Sciences Ltd. advance its pipeline?
What additional initiatives does Roivant Sciences Ltd. undertake?