Nvidia Set for Potential 33% Surge? Check Out 10 Leading Analyst Predictions for Monday
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Aug 18 2025
0mins
Should l Buy PSTV?
Source: Benzinga
Analyst Upgrades and Downgrades: Various Wall Street analysts have adjusted their price targets and ratings for several companies, reflecting changes in market outlook.
Bitdeer Technologies Group: HC Wainwright & Co. raised the price target from $18 to $19 while maintaining a Buy rating; shares closed at $13.39.
Luminar Technologies: Goldman Sachs reduced the price target from $2 to $1 with a Sell rating; shares closed at $2.30.
NVIDIA Corporation: Cantor Fitzgerald increased the price target from $200 to $240, keeping an Overweight rating; shares closed at $180.45.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy PSTV?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on PSTV
Wall Street analysts forecast PSTV stock price to rise
3 Analyst Rating
3 Buy
0 Hold
0 Sell
Strong Buy
Current: 6.390
Low
2.00
Averages
8.00
High
19.00
Current: 6.390
Low
2.00
Averages
8.00
High
19.00
About PSTV
Plus Therapeutics, Inc. is a clinical-stage pharmaceutical company. The Company is engaged in developing targeted radiotherapeutics for difficult-to-treat cancers of the central nervous system. Combining image-guided local beta radiation and targeted drug delivery approaches, it is advancing a pipeline of product candidates with lead programs in leptomeningeal metastases (LM) and recurrent glioblastoma (GBM). Its lead radiotherapeutic candidate, REYOBIQ (rhenium (186Re) obisbemeda), is designed specifically for CNS cancers including GBM, LM, and pediatric brain cancers (PBC) by direct localized delivery utilizing approved standard-of-care tissue access such as with convection-enhanced delivery (CED) and intraventricular brain (Ommaya reservoir) catheters. Its radiotherapeutic candidate, Rhenium-188 NanoLiposome Biodegradable Alginate Microsphere (188RNL-BAM), is designed to treat many solid organ cancers including primary and secondary liver cancers via intra-arterial injections.
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.
Plus Therapeutics Stock Meets Nasdaq Minimum Bid Requirement
- Stock Price Compliance: Plus Therapeutics (PSTV) announced that its common stock has once again met Nasdaq's minimum bid requirement, with the closing price remaining above $1.00 per share for 10 consecutive trading days, indicating stability and market acceptance of the company's stock.
- Price Movement: PSTV's stock price rose approximately 2.9% in pre-market trading on Tuesday, reflecting a positive investor response to the latest announcement, which may enhance market confidence and attract more investor interest.
- Financial Performance Beat: Plus Therapeutics reported a GAAP EPS of -$0.29, beating expectations by $0.01, while revenue reached $5.21 million, exceeding forecasts by $0.14 million, demonstrating improvements in financial management and operational efficiency.
- Clinical Program Progress: The company's advancements in the REYOBIQ clinical program have also garnered market attention, indicating ongoing efforts in drug development that could lay the groundwork for future revenue growth.
See More
Plus Therapeutics Regains Nasdaq Compliance with Minimum Bid Price
- Compliance Regained: Plus Therapeutics has received confirmation from Nasdaq that it has regained compliance with the minimum bid price requirement, as its stock closed at or above $1.00 per share for 10 consecutive business days from April 6 to April 17, 2026, indicating enhanced stability in the capital markets.
- Investor Confidence Boost: This compliance restoration not only eliminates potential delisting risks but also may bolster investor confidence in the company's future growth, particularly given its focus on developing precision diagnostics and radiopharmaceuticals for CNS cancers.
- Strategic Partnership Network: Plus Therapeutics has established a supply chain through strategic partnerships that support the development and future commercialization of its targeted radiotherapeutics for difficult-to-treat cancers, showcasing its competitive edge and market potential in the industry.
- Broad Clinical Prospects: The company is advancing its pipeline of product candidates targeting leptomeningeal metastases and recurrent glioblastoma, utilizing image-guided local beta radiation and targeted drug delivery approaches, which are expected to significantly enhance clinical outcomes and further solidify its market position.
See More
Plus Therapeutics Appoints New VP of Value Strategy
- Executive Appointment: Plus Therapeutics appointed Dr. Randy H. Goodman as Vice President of Value Strategy & Health Economics on April 13, 2026, leveraging over 20 years of experience in biotechnology and pharmaceuticals to enhance market access and value strategies in CNS cancers.
- Market Access Strategy: Dr. Goodman will lead the development and implementation of market access strategies aimed at supporting the commercial expansion of CNSide and REYOBIQ, ensuring their clinical and economic value is clearly articulated within the healthcare system to enhance product competitiveness.
- Equity Incentive Plan: As an inducement to join the company, Dr. Goodman was granted 9,000 shares of common stock, including 4,500 stock options and 4,500 restricted stock units (RSUs), with an exercise price of $5.41 per share and a 10-year term.
- Industry Influence: Having advised leading global healthcare organizations like Pfizer, Gilead Sciences, and Moderna, Dr. Goodman's expertise in health policy and value-based pricing will provide critical support for Plus Therapeutics in navigating the complex healthcare landscape.
See More
Plus Appoints New Chief Development Officer and Receives FDA Approval
- Executive Appointment: Plus Therapeutics has appointed Eric J. Daniels as Chief Development Officer effective April 20, with Daniels previously serving as CDO at Kiora Pharmaceuticals, overseeing clinical and manufacturing activities, aiming to enhance the company's R&D capabilities for future product development.
- FDA Approval: The company received FDA approval to evaluate its experimental therapy REYOBIQ in pediatric patients with high-grade glioma and ependymoma, marking a strategic expansion into pediatric oncology that could open new market opportunities for the company.
- Stock Performance: Shares of Plus Therapeutics surged 24% following the announcement of the new CDO and the FDA granting orphan drug designation, indicating strong market optimism about the company's future prospects, potentially leading to its best week since late September if gains hold.
- Orphan Drug Designation: REYOBIQ's orphan drug designation provides several potential benefits, including tax credits and fee waivers, which will help reduce R&D costs and enhance the product's competitive position in the market.
See More
Plus Therapeutics Appoints New Chief Development Officer
- Executive Appointment: Plus Therapeutics announced the appointment of Eric J. Daniels, M.D., MBA, as Chief Development Officer effective April 20, 2026, aimed at accelerating product development in the central nervous system cancer sector.
- Extensive Experience: Daniels brings over 20 years of biotechnology experience, having served as Chief Development Officer at Kiora Pharmaceuticals, where he oversaw the entire development portfolio, showcasing his deep background in clinical development and regulatory strategy.
- Strategic Importance: His addition is seen as crucial for advancing REYOBIQ and the broader CNS oncology portfolio, with Plus Therapeutics expecting to enhance the clinical and commercial viability of its products through his expertise.
- Innovative Platform: The company focuses on developing targeted radiotherapeutic platforms for difficult-to-treat CNS cancers, and Daniels' leadership is anticipated to lead to improved patient outcomes, further solidifying the company's market position.
See More
Plus Therapeutics Receives FDA Orphan Drug Designation
- Orphan Drug Designation: Plus Therapeutics' REYOBIQ™ has received Orphan Drug Designation from the FDA for treating pediatric malignant gliomas, marking a significant milestone that supports the company's innovation in rare cancer treatments.
- Market Exclusivity: This designation grants REYOBIQ seven years of market exclusivity, potentially enhancing the company's competitive position in the pediatric cancer treatment market while providing tax incentives for future clinical trials.
- Accelerated Clinical Progress: The orphan drug designation is based on positive clinical data for REYOBIQ in pediatric high-grade gliomas and ependymomas, indicating the drug's potential to improve patient outcomes, especially where existing treatment options are limited.
- Research Funding Support: The company has also received FDA approval for its Investigational New Drug application for REYOBIQ, further advancing its clinical research in pediatric high-grade gliomas and ependymomas, demonstrating ongoing development potential in CNS tumor treatments.
See More
Plus Therapeutics Stock Meets Nasdaq Minimum Bid Requirement
- Stock Price Compliance: Plus Therapeutics (PSTV) announced that its common stock has once again met Nasdaq's minimum bid requirement, with the closing price remaining above $1.00 per share for 10 consecutive trading days, indicating stability and market acceptance of the company's stock.
- Price Movement: PSTV's stock price rose approximately 2.9% in pre-market trading on Tuesday, reflecting a positive investor response to the latest announcement, which may enhance market confidence and attract more investor interest.
- Financial Performance Beat: Plus Therapeutics reported a GAAP EPS of -$0.29, beating expectations by $0.01, while revenue reached $5.21 million, exceeding forecasts by $0.14 million, demonstrating improvements in financial management and operational efficiency.
- Clinical Program Progress: The company's advancements in the REYOBIQ clinical program have also garnered market attention, indicating ongoing efforts in drug development that could lay the groundwork for future revenue growth.
See More
Plus Therapeutics Regains Nasdaq Compliance with Minimum Bid Price
- Compliance Regained: Plus Therapeutics has received confirmation from Nasdaq that it has regained compliance with the minimum bid price requirement, as its stock closed at or above $1.00 per share for 10 consecutive business days from April 6 to April 17, 2026, indicating enhanced stability in the capital markets.
- Investor Confidence Boost: This compliance restoration not only eliminates potential delisting risks but also may bolster investor confidence in the company's future growth, particularly given its focus on developing precision diagnostics and radiopharmaceuticals for CNS cancers.
- Strategic Partnership Network: Plus Therapeutics has established a supply chain through strategic partnerships that support the development and future commercialization of its targeted radiotherapeutics for difficult-to-treat cancers, showcasing its competitive edge and market potential in the industry.
- Broad Clinical Prospects: The company is advancing its pipeline of product candidates targeting leptomeningeal metastases and recurrent glioblastoma, utilizing image-guided local beta radiation and targeted drug delivery approaches, which are expected to significantly enhance clinical outcomes and further solidify its market position.
See More
Plus Therapeutics Appoints New VP of Value Strategy
- Executive Appointment: Plus Therapeutics appointed Dr. Randy H. Goodman as Vice President of Value Strategy & Health Economics on April 13, 2026, leveraging over 20 years of experience in biotechnology and pharmaceuticals to enhance market access and value strategies in CNS cancers.
- Market Access Strategy: Dr. Goodman will lead the development and implementation of market access strategies aimed at supporting the commercial expansion of CNSide and REYOBIQ, ensuring their clinical and economic value is clearly articulated within the healthcare system to enhance product competitiveness.
- Equity Incentive Plan: As an inducement to join the company, Dr. Goodman was granted 9,000 shares of common stock, including 4,500 stock options and 4,500 restricted stock units (RSUs), with an exercise price of $5.41 per share and a 10-year term.
- Industry Influence: Having advised leading global healthcare organizations like Pfizer, Gilead Sciences, and Moderna, Dr. Goodman's expertise in health policy and value-based pricing will provide critical support for Plus Therapeutics in navigating the complex healthcare landscape.
See More
Plus Appoints New Chief Development Officer and Receives FDA Approval
- Executive Appointment: Plus Therapeutics has appointed Eric J. Daniels as Chief Development Officer effective April 20, with Daniels previously serving as CDO at Kiora Pharmaceuticals, overseeing clinical and manufacturing activities, aiming to enhance the company's R&D capabilities for future product development.
- FDA Approval: The company received FDA approval to evaluate its experimental therapy REYOBIQ in pediatric patients with high-grade glioma and ependymoma, marking a strategic expansion into pediatric oncology that could open new market opportunities for the company.
- Stock Performance: Shares of Plus Therapeutics surged 24% following the announcement of the new CDO and the FDA granting orphan drug designation, indicating strong market optimism about the company's future prospects, potentially leading to its best week since late September if gains hold.
- Orphan Drug Designation: REYOBIQ's orphan drug designation provides several potential benefits, including tax credits and fee waivers, which will help reduce R&D costs and enhance the product's competitive position in the market.
See More
Plus Therapeutics Appoints New Chief Development Officer
- Executive Appointment: Plus Therapeutics announced the appointment of Eric J. Daniels, M.D., MBA, as Chief Development Officer effective April 20, 2026, aimed at accelerating product development in the central nervous system cancer sector.
- Extensive Experience: Daniels brings over 20 years of biotechnology experience, having served as Chief Development Officer at Kiora Pharmaceuticals, where he oversaw the entire development portfolio, showcasing his deep background in clinical development and regulatory strategy.
- Strategic Importance: His addition is seen as crucial for advancing REYOBIQ and the broader CNS oncology portfolio, with Plus Therapeutics expecting to enhance the clinical and commercial viability of its products through his expertise.
- Innovative Platform: The company focuses on developing targeted radiotherapeutic platforms for difficult-to-treat CNS cancers, and Daniels' leadership is anticipated to lead to improved patient outcomes, further solidifying the company's market position.
See More
Plus Therapeutics Receives FDA Orphan Drug Designation
- Orphan Drug Designation: Plus Therapeutics' REYOBIQ™ has received Orphan Drug Designation from the FDA for treating pediatric malignant gliomas, marking a significant milestone that supports the company's innovation in rare cancer treatments.
- Market Exclusivity: This designation grants REYOBIQ seven years of market exclusivity, potentially enhancing the company's competitive position in the pediatric cancer treatment market while providing tax incentives for future clinical trials.
- Accelerated Clinical Progress: The orphan drug designation is based on positive clinical data for REYOBIQ in pediatric high-grade gliomas and ependymomas, indicating the drug's potential to improve patient outcomes, especially where existing treatment options are limited.
- Research Funding Support: The company has also received FDA approval for its Investigational New Drug application for REYOBIQ, further advancing its clinical research in pediatric high-grade gliomas and ependymomas, demonstrating ongoing development potential in CNS tumor treatments.
See More
