Citi and H.C. Wainwright Raise Roivant Sciences Price Targets Following Positive Drug Data
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Feb 14 2026
0mins
Should l Buy ROIV?
Source: Yahoo Finance
- Price Target Increases: Citi raised Roivant Sciences' price target from $26 to $35 while maintaining a Buy rating, primarily based on positive Phase 2 data for brepocitinib in cutaneous sarcoidosis, indicating strong growth potential for the drug.
- Impressive Data Performance: H.C. Wainwright also increased Roivant's price target from $26 to $33, emphasizing the impressive Phase 2 data and incorporating this indication into their valuation model, reflecting growing market confidence in the drug.
- Bank Rating Changes: Prior to this, Bank of America raised Roivant's price target from $22 to $26 with a Neutral rating, noting that FQ3 2026 results were in line with expectations and highlighting the positive topline results for brepocitinib.
- Optimistic Market Outlook: With analysts raising sales forecasts for brepocitinib, Roivant Sciences' market outlook is generally positive, showcasing the company's potential and investment value in the biopharmaceutical sector.
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Analyst Views on ROIV
Wall Street analysts forecast ROIV stock price to fall
8 Analyst Rating
7 Buy
1 Hold
0 Sell
Strong Buy
Current: 28.100
Low
22.00
Averages
27.63
High
33.00
Current: 28.100
Low
22.00
Averages
27.63
High
33.00
About ROIV
Roivant Sciences Ltd. is a biopharmaceutical company focused on improving the lives of patients by accelerating the development and commercialization of medicines that matter. The Company’s pipeline includes brepocitinib, a potent small molecule inhibitor of TYK2 and JAK1 in development for the treatment of dermatomyositis, non-infectious uveitis and cutaneous sarcoidosis; IMVT-1402 and batoclimab, fully human monoclonal antibodies targeting FcRn in development across several IgG-mediated autoimmune indications; and mosliciguat, an inhaled sGC activator in development for pulmonary hypertension associated with interstitial lung disease. It also incubates discovery-stage companies and health technology startups complementary to its biopharmaceutical business.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Priovant Secures FDA Priority Review for Brepocitinib
- FDA Priority Review: Priovant Therapeutics announced that its drug brepocitinib for dermatomyositis has received priority review from the FDA, marking a significant advancement in the treatment of rare diseases and potentially accelerating the drug's market entry.
- Clinical Trial Results: The New Drug Application is supported by data from the Phase 3 VALOR study involving 241 patients, where brepocitinib at a 30 mg dose demonstrated statistically significant improvement in the myositis Total Improvement Score, achieving the study's primary endpoint and enhancing the likelihood of FDA approval.
- Market Potential: If approved, brepocitinib will be the first FDA-approved targeted therapy for dermatomyositis, expected to fill a market gap and meet the urgent need for effective treatments, thereby enhancing Priovant's market position.
- Company Commitment: Priovant CEO Ben Zimmer stated that the company is committed to working closely with the FDA to expedite the drug's availability, reflecting its strong focus on patient welfare and proactive engagement with market opportunities.
See More
Priovant's Dermatomyositis Drug Receives FDA Priority Review
- FDA Review Progress: Priovant Therapeutics' brepocitinib has received Priority Review from the FDA, with a target action date in Q3 2026, and if approved, it will be the first targeted therapy for dermatomyositis, addressing urgent patient needs.
- Clinical Trial Results: The Phase 3 VALOR study demonstrated significant efficacy of brepocitinib in 241 patients, with the 30 mg dose showing statistically significant improvement in the Myositis Total Improvement Score (TIS) at 52 weeks compared to placebo, indicating its potential to enhance patient quality of life.
- Market Potential: If approved, brepocitinib will provide a new treatment option for dermatomyositis patients who have long relied on high-dose steroids, potentially reducing disease burden and improving quality of life significantly.
- Company Commitment: Priovant CEO Ben Zimmer emphasized the company's commitment to working closely with the FDA to expedite the drug's availability, reflecting a strong dedication to meeting the needs of dermatomyositis patients.
See More
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- Price Target Increases: Citi raised Roivant Sciences' price target from $26 to $35 while maintaining a Buy rating, primarily based on positive Phase 2 data for brepocitinib in cutaneous sarcoidosis, indicating strong growth potential for the drug.
- Impressive Data Performance: H.C. Wainwright also increased Roivant's price target from $26 to $33, emphasizing the impressive Phase 2 data and incorporating this indication into their valuation model, reflecting growing market confidence in the drug.
- Bank Rating Changes: Prior to this, Bank of America raised Roivant's price target from $22 to $26 with a Neutral rating, noting that FQ3 2026 results were in line with expectations and highlighting the positive topline results for brepocitinib.
- Optimistic Market Outlook: With analysts raising sales forecasts for brepocitinib, Roivant Sciences' market outlook is generally positive, showcasing the company's potential and investment value in the biopharmaceutical sector.
See More
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- FDA Priority Review: Priovant Therapeutics announced that its drug brepocitinib for dermatomyositis has received priority review from the FDA, marking a significant advancement in the treatment of rare diseases and potentially accelerating the drug's market entry.
- Clinical Trial Results: The New Drug Application is supported by data from the Phase 3 VALOR study involving 241 patients, where brepocitinib at a 30 mg dose demonstrated statistically significant improvement in the myositis Total Improvement Score, achieving the study's primary endpoint and enhancing the likelihood of FDA approval.
- Market Potential: If approved, brepocitinib will be the first FDA-approved targeted therapy for dermatomyositis, expected to fill a market gap and meet the urgent need for effective treatments, thereby enhancing Priovant's market position.
- Company Commitment: Priovant CEO Ben Zimmer stated that the company is committed to working closely with the FDA to expedite the drug's availability, reflecting its strong focus on patient welfare and proactive engagement with market opportunities.
See More
Priovant's Dermatomyositis Drug Receives FDA Priority Review
- FDA Review Progress: Priovant Therapeutics' brepocitinib has received Priority Review from the FDA, with a target action date in Q3 2026, and if approved, it will be the first targeted therapy for dermatomyositis, addressing urgent patient needs.
- Clinical Trial Results: The Phase 3 VALOR study demonstrated significant efficacy of brepocitinib in 241 patients, with the 30 mg dose showing statistically significant improvement in the Myositis Total Improvement Score (TIS) at 52 weeks compared to placebo, indicating its potential to enhance patient quality of life.
- Market Potential: If approved, brepocitinib will provide a new treatment option for dermatomyositis patients who have long relied on high-dose steroids, potentially reducing disease burden and improving quality of life significantly.
- Company Commitment: Priovant CEO Ben Zimmer emphasized the company's commitment to working closely with the FDA to expedite the drug's availability, reflecting a strong dedication to meeting the needs of dermatomyositis patients.
See More
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- Stake Increase: Perceptive Advisors purchased an additional 203,881 shares of Celcuity in Q4 2026, with an estimated transaction value of $16.76 million, indicating strong confidence in the company's future growth potential.
- Ownership Proportion Rise: Following this purchase, Perceptive Advisors' stake in Celcuity increased to 5.62%, highlighting its significance within the investment portfolio and further drawing market attention to Celcuity.
- Market Performance: As of February 17, 2026, Celcuity shares were priced at $107.32, reflecting a staggering 700% increase over the past year, underscoring strong market anticipation for its drug development.
- FDA Review Progress: Celcuity's new drug application for gedatolisib has received Priority Review from the FDA, with a decision expected by July 17, 2026, a critical timeline that could significantly impact its future market performance.
See More
Roivant Sciences (ROIV.US) Officer Plans to Sell $44.03 Million in Common Stock via Form 144
Stock Sale Announcement: Officer Frank Torti plans to sell 1.6 million shares of Roivant Sciences common stock on February 20, with a total market value of approximately $44.03 million.
Shareholding Reduction: Frank Torti has reduced his shareholding in Roivant Sciences by 1.4 million shares since February 19, 2026, with a total value of around $38.39 million.
See More
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- Investment Strategy Shift: David Einhorn invested tens of millions in Q4 2025 to increase stakes in Graphic Packaging and Capri Holdings by over 70%, reflecting his concerns about AI-driven market overvaluation and indicating a strategic pivot away from big tech.
- Stock Performance Volatility: Despite Graphic Packaging's shares dropping about 23% in Q4 2025 and over 44% for the year, Wall Street analysts remain optimistic, with an average price target suggesting more than 35% upside, indicating expectations for a rebound in the stock.
- Healthcare Investments: Einhorn more than doubled his position in Acadia Healthcare to over $58 million, despite a 43% plunge in Q4; however, analysts maintain a buy rating with a price target suggesting over 16% upside in the next 12 months, reflecting confidence in its recovery.
- Cautious on Tech Stocks: While expressing concerns about tech valuations, Einhorn established a $35 million stake in Global Payments, which fell 31% in 2025 but rebounded nearly 5% in 2026, with analysts' price targets implying over 25% upside, suggesting market optimism for its future performance.
See More
Citi and H.C. Wainwright Raise Roivant Sciences Price Targets Following Positive Drug Data
- Price Target Increases: Citi raised Roivant Sciences' price target from $26 to $35 while maintaining a Buy rating, primarily based on positive Phase 2 data for brepocitinib in cutaneous sarcoidosis, indicating strong growth potential for the drug.
- Impressive Data Performance: H.C. Wainwright also increased Roivant's price target from $26 to $33, emphasizing the impressive Phase 2 data and incorporating this indication into their valuation model, reflecting growing market confidence in the drug.
- Bank Rating Changes: Prior to this, Bank of America raised Roivant's price target from $22 to $26 with a Neutral rating, noting that FQ3 2026 results were in line with expectations and highlighting the positive topline results for brepocitinib.
- Optimistic Market Outlook: With analysts raising sales forecasts for brepocitinib, Roivant Sciences' market outlook is generally positive, showcasing the company's potential and investment value in the biopharmaceutical sector.
See More
