Analysts Predict SCHX Will Hit $28
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Aug 25 2025
0mins
Should l Buy ROIV?
Source: NASDAQ.COM
ETF Analysis: The Schwab US Large-Cap ETF (SCHX) has an implied analyst target price of $28.23 per unit, indicating a potential upside of 10.46% from its current trading price of $25.56.
Notable Holdings: Key underlying holdings with significant upside include Atlassian Corp (TEAM), Repligen Corp (RGEN), and Roivant Sciences Ltd (ROIV), with expected increases of 44.73%, 44.01%, and 43.55% respectively.
Market Sentiment: Analysts' optimistic target prices may reflect future expectations but could also lead to downgrades if they are based on outdated information or fail to account for recent developments.
Investor Consideration: Investors are encouraged to conduct further research to determine the validity of analysts' targets and whether they align with current market conditions.
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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: 28.360
Low
22.00
Averages
27.63
High
33.00
Current: 28.360
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.
Moderna Surpasses Q1 Revenue Estimates Driven by International Vaccine Sales
- International Revenue Surge: Moderna's Q1 international revenue reached $311 million, significantly outpacing the $78 million from U.S. markets, demonstrating strong sales driven by partnerships in the UK, Canada, and Australia, thereby balancing its revenue structure between international and domestic markets.
- Vaccine Policy Impact: Major changes in U.S. vaccine policy have led to reduced vaccine usage, with Moderna's CFO expressing hope for a more stable market moving forward, anticipating a recovery in the U.S. COVID market by 2026, which will influence the company's long-term strategy.
- Strong Financial Performance: Moderna reported Q1 revenue of $389 million, an increase of $281 million year-over-year, exceeding analysts' expectations of $228 million, indicating robust performance in the vaccine market and a recovery in demand.
- New Product Development: The company is expanding its product line with plans for an mRNA flu vaccine and developing a personalized cancer vaccine in partnership with Merck, as well as treatments for rare metabolic disorders, showcasing its strategic shift in the post-pandemic era.
See More
Roivant Sciences (ROIV.US) Officer Plans to Sell $8.45 Million in Common Stock via Form 144 Amendment
Share Sale Announcement: Glene Matthew intends to sell 289,777 shares of Roivant Sciences, valued at approximately $8.45 million.
Reduction in Holdings: Glene Matthew has decreased his shareholding in Roivant Sciences by 358,511 shares since March 30, 2026, with a total value of around $9.86 million.
See More
Priovant Launches Phase 2b/3 Trial for Lichen Planopilaris
- Trial Launch: Priovant commenced enrollment of the first subjects in a seamless Phase 2b/3 clinical trial for Lichen Planopilaris (LPP) in March 2026, marking the fourth indication in its late-stage development program and demonstrating the company's ongoing commitment to addressing high-morbidity autoimmune diseases.
- Urgent Market Need: LPP affects approximately 100,000 adults in the U.S., causing irreversible hair loss and permanent scarring, with no FDA-approved therapies available, highlighting Priovant's strategic importance in fulfilling this critical therapeutic gap.
- Drug Development Progress: Brepocitinib, a selective TYK2 and JAK1 inhibitor, has generated positive Phase 3 data in dermatomyositis, with its New Drug Application currently under FDA review, expected to receive approval in Q3 2026, further enhancing its potential in multi-indication development.
- Strategic Positioning: Priovant's CEO noted that expanding Brepocitinib into LPP aligns with its strategy in developing therapies for highly morbid orphan conditions, anticipating synergistic effects with the upcoming product launch in dermatomyositis to strengthen market competitiveness.
See More
Roivant Launches New Clinical Trial for LPP
- New Clinical Trial Launch: Roivant initiated a seamless Phase 2b/3 clinical trial for Lichen planopilaris (LPP) in March 2026, marking the fourth indication in its late-stage development program, demonstrating the company's proactive approach to addressing critical unmet therapeutic needs.
- FDA Priority Review: The FDA has granted Priority Review for the New Drug Application (NDA) of brepocitinib, with a target action date expected in Q3 2026, potentially accelerating market access for this treatment to meet urgent patient needs in LPP.
- Clinical Data Support: Strong mechanistic rationale and clinically meaningful results from an investigator-initiated placebo-controlled study support the rapid development of brepocitinib in LPP, highlighting its potential efficacy in this challenging condition.
- Multi-Indication Strategy: CEO Ben Zimmer emphasized that expanding brepocitinib into LPP aligns with the company's strategy of developing treatments for highly morbid orphan conditions, anticipating synergistic effects with other indications like dermatomyositis to enhance market competitiveness.
See More
S&P 500 Futures Rise in Pre-Market Session; United Therapeutics and Alcoa Take the Lead
Market Opening: U.S. stock markets are set to open in two hours.
United Therapeutics Corp. Performance: United Therapeutics Corp. (UTHR) saw a 12.9% increase in pre-market trading.
Alcoa Corp. Performance: Alcoa Corp. (AA) experienced a 9.3% rise in pre-market trading.
Overall Market Sentiment: The pre-market gains indicate positive sentiment among investors for these companies.
See More
Brepocitinib Shows Significant Benefits in Dermatomyositis Trial
- Clinical Trial Results: The Phase 3 VALOR trial demonstrated that brepocitinib 30 mg achieved a 15.3-point improvement in the Total Improvement Score (TIS) at Week 52 compared to placebo (P<0.001), indicating significant clinical benefits and potential in treating dermatomyositis.
- Adverse Event Management: Although the incidence of serious infections was higher in the brepocitinib 30 mg group compared to placebo, these events were resolved with medical management, and most patients completed treatment, suggesting a manageable safety profile.
- FDA Priority Review: The U.S. FDA has granted Priority Review for brepocitinib's New Drug Application (NDA) with a target action date set for Q3 2026, which could provide a new treatment option for patients with dermatomyositis if approved.
- Improvement in Quality of Life: Data presented at the AAD 2026 meeting indicated that 18.9% of patients in the brepocitinib 30 mg group achieved itch remission by Week 4, with sustained improvements in skin-related quality of life throughout the 52-week trial, highlighting its potential to enhance patient quality of life.
See More
Moderna Surpasses Q1 Revenue Estimates Driven by International Vaccine Sales
- International Revenue Surge: Moderna's Q1 international revenue reached $311 million, significantly outpacing the $78 million from U.S. markets, demonstrating strong sales driven by partnerships in the UK, Canada, and Australia, thereby balancing its revenue structure between international and domestic markets.
- Vaccine Policy Impact: Major changes in U.S. vaccine policy have led to reduced vaccine usage, with Moderna's CFO expressing hope for a more stable market moving forward, anticipating a recovery in the U.S. COVID market by 2026, which will influence the company's long-term strategy.
- Strong Financial Performance: Moderna reported Q1 revenue of $389 million, an increase of $281 million year-over-year, exceeding analysts' expectations of $228 million, indicating robust performance in the vaccine market and a recovery in demand.
- New Product Development: The company is expanding its product line with plans for an mRNA flu vaccine and developing a personalized cancer vaccine in partnership with Merck, as well as treatments for rare metabolic disorders, showcasing its strategic shift in the post-pandemic era.
See More
Roivant Sciences (ROIV.US) Officer Plans to Sell $8.45 Million in Common Stock via Form 144 Amendment
Share Sale Announcement: Glene Matthew intends to sell 289,777 shares of Roivant Sciences, valued at approximately $8.45 million.
Reduction in Holdings: Glene Matthew has decreased his shareholding in Roivant Sciences by 358,511 shares since March 30, 2026, with a total value of around $9.86 million.
See More
Priovant Launches Phase 2b/3 Trial for Lichen Planopilaris
- Trial Launch: Priovant commenced enrollment of the first subjects in a seamless Phase 2b/3 clinical trial for Lichen Planopilaris (LPP) in March 2026, marking the fourth indication in its late-stage development program and demonstrating the company's ongoing commitment to addressing high-morbidity autoimmune diseases.
- Urgent Market Need: LPP affects approximately 100,000 adults in the U.S., causing irreversible hair loss and permanent scarring, with no FDA-approved therapies available, highlighting Priovant's strategic importance in fulfilling this critical therapeutic gap.
- Drug Development Progress: Brepocitinib, a selective TYK2 and JAK1 inhibitor, has generated positive Phase 3 data in dermatomyositis, with its New Drug Application currently under FDA review, expected to receive approval in Q3 2026, further enhancing its potential in multi-indication development.
- Strategic Positioning: Priovant's CEO noted that expanding Brepocitinib into LPP aligns with its strategy in developing therapies for highly morbid orphan conditions, anticipating synergistic effects with the upcoming product launch in dermatomyositis to strengthen market competitiveness.
See More
Roivant Launches New Clinical Trial for LPP
- New Clinical Trial Launch: Roivant initiated a seamless Phase 2b/3 clinical trial for Lichen planopilaris (LPP) in March 2026, marking the fourth indication in its late-stage development program, demonstrating the company's proactive approach to addressing critical unmet therapeutic needs.
- FDA Priority Review: The FDA has granted Priority Review for the New Drug Application (NDA) of brepocitinib, with a target action date expected in Q3 2026, potentially accelerating market access for this treatment to meet urgent patient needs in LPP.
- Clinical Data Support: Strong mechanistic rationale and clinically meaningful results from an investigator-initiated placebo-controlled study support the rapid development of brepocitinib in LPP, highlighting its potential efficacy in this challenging condition.
- Multi-Indication Strategy: CEO Ben Zimmer emphasized that expanding brepocitinib into LPP aligns with the company's strategy of developing treatments for highly morbid orphan conditions, anticipating synergistic effects with other indications like dermatomyositis to enhance market competitiveness.
See More
S&P 500 Futures Rise in Pre-Market Session; United Therapeutics and Alcoa Take the Lead
Market Opening: U.S. stock markets are set to open in two hours.
United Therapeutics Corp. Performance: United Therapeutics Corp. (UTHR) saw a 12.9% increase in pre-market trading.
Alcoa Corp. Performance: Alcoa Corp. (AA) experienced a 9.3% rise in pre-market trading.
Overall Market Sentiment: The pre-market gains indicate positive sentiment among investors for these companies.
See More
Brepocitinib Shows Significant Benefits in Dermatomyositis Trial
- Clinical Trial Results: The Phase 3 VALOR trial demonstrated that brepocitinib 30 mg achieved a 15.3-point improvement in the Total Improvement Score (TIS) at Week 52 compared to placebo (P<0.001), indicating significant clinical benefits and potential in treating dermatomyositis.
- Adverse Event Management: Although the incidence of serious infections was higher in the brepocitinib 30 mg group compared to placebo, these events were resolved with medical management, and most patients completed treatment, suggesting a manageable safety profile.
- FDA Priority Review: The U.S. FDA has granted Priority Review for brepocitinib's New Drug Application (NDA) with a target action date set for Q3 2026, which could provide a new treatment option for patients with dermatomyositis if approved.
- Improvement in Quality of Life: Data presented at the AAD 2026 meeting indicated that 18.9% of patients in the brepocitinib 30 mg group achieved itch remission by Week 4, with sustained improvements in skin-related quality of life throughout the 52-week trial, highlighting its potential to enhance patient quality of life.
See More
