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.
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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: 3.920
Low
2.00
Averages
8.00
High
19.00
Current: 3.920
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 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 Secures New CPT Code for CNSide Test
- New CPT Code Approval: The American Medical Association has approved a proprietary laboratory analysis code 0640U for Plus Therapeutics' CNSide CSF Tumor Cell Enumeration test, effective July 1, 2026, marking a significant milestone in the company's U.S. commercialization efforts and expected to facilitate broader clinical adoption.
- Streamlined Reimbursement Process: The implementation of the new code simplifies the reimbursement pathway for oncologists and neurologists managing patients with suspected leptomeningeal metastases, thereby enhancing the clinical adoption rate of the CNSide test and strengthening the company's market position in CNS cancer management.
- Facilitating Clinical Adoption: By providing a dedicated billing code, the CNSide test will benefit from standardized claims submission, which not only aids in increasing physician utilization but also supports tracking of test utilization through real-world evidence generation, further driving market acceptance.
- Advancing Commercial Strategy: This coding milestone reinforces Plus Therapeutics' commercial foundation in the U.S. market, which is anticipated to contribute significantly to revenue growth while also supporting the expansion of its therapeutic pipeline.
See More
Plus Therapeutics Secures New Payer Agreement with Highmark
- Expanded Coverage: The agreement with Highmark increases the total covered lives for Plus Therapeutics' CNSide® Tumor Cell Enumeration assay from 67 million to 75 million, making significant progress towards the company's goal of 150 million covered lives by 2026, thereby enhancing patient access across the U.S.
- Reduced Reimbursement Barriers: This agreement is expected to accelerate the adoption of CNSide in oncology centers by lowering reimbursement barriers for ordering physicians, thereby strengthening the company's competitive position in the oncology diagnostics market.
- Clinical Utility Validation: The CNSide® assay has demonstrated superior clinical utility over conventional CSF cytology in nine peer-reviewed publications and the FORESEE clinical trial, enabling earlier and more accurate detection and monitoring of leptomeningeal metastases, which optimizes treatment strategies.
- Significant Economic Benefits: Health economic analyses indicate that early detection with CNSide can reduce overall healthcare costs related to leptomeningeal metastases by approximately 40%, driven by earlier diagnosis and treatment optimization, ultimately improving patient outcomes.
See More
Plus Therapeutics Grants Inducement Awards to New Employees
- Inducement Awards Granted: Plus Therapeutics granted a total of 300,000 stock options and 300,000 restricted stock units (RSUs) to two new employees on March 26, 2026, aimed at attracting top talent and strengthening the team.
- Option Details: The options have a 10-year term with an exercise price of $0.243 per share, reflecting the fair market value on the grant date, and will vest over four years, with 25% vesting on the first anniversary and 1/36 vesting monthly thereafter.
- RSU Vesting Schedule: Each RSU represents a contingent right to one share of common stock, vesting over three years with 1/3 vesting on the first anniversary and the remainder vesting ratably over the next eight quarters, contingent on continued service with the company.
- Compliance Approval: The awards were approved by the Compensation Committee of the board, ensuring compliance with Nasdaq Rule 5635(c)(4), which reinforces the effectiveness of the inducement measures and strengthens the company's position in the industry.
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 Secures New CPT Code for CNSide Test
- New CPT Code Approval: The American Medical Association has approved a proprietary laboratory analysis code 0640U for Plus Therapeutics' CNSide CSF Tumor Cell Enumeration test, effective July 1, 2026, marking a significant milestone in the company's U.S. commercialization efforts and expected to facilitate broader clinical adoption.
- Streamlined Reimbursement Process: The implementation of the new code simplifies the reimbursement pathway for oncologists and neurologists managing patients with suspected leptomeningeal metastases, thereby enhancing the clinical adoption rate of the CNSide test and strengthening the company's market position in CNS cancer management.
- Facilitating Clinical Adoption: By providing a dedicated billing code, the CNSide test will benefit from standardized claims submission, which not only aids in increasing physician utilization but also supports tracking of test utilization through real-world evidence generation, further driving market acceptance.
- Advancing Commercial Strategy: This coding milestone reinforces Plus Therapeutics' commercial foundation in the U.S. market, which is anticipated to contribute significantly to revenue growth while also supporting the expansion of its therapeutic pipeline.
See More
Plus Therapeutics Secures New Payer Agreement with Highmark
- Expanded Coverage: The agreement with Highmark increases the total covered lives for Plus Therapeutics' CNSide® Tumor Cell Enumeration assay from 67 million to 75 million, making significant progress towards the company's goal of 150 million covered lives by 2026, thereby enhancing patient access across the U.S.
- Reduced Reimbursement Barriers: This agreement is expected to accelerate the adoption of CNSide in oncology centers by lowering reimbursement barriers for ordering physicians, thereby strengthening the company's competitive position in the oncology diagnostics market.
- Clinical Utility Validation: The CNSide® assay has demonstrated superior clinical utility over conventional CSF cytology in nine peer-reviewed publications and the FORESEE clinical trial, enabling earlier and more accurate detection and monitoring of leptomeningeal metastases, which optimizes treatment strategies.
- Significant Economic Benefits: Health economic analyses indicate that early detection with CNSide can reduce overall healthcare costs related to leptomeningeal metastases by approximately 40%, driven by earlier diagnosis and treatment optimization, ultimately improving patient outcomes.
See More
Plus Therapeutics Grants Inducement Awards to New Employees
- Inducement Awards Granted: Plus Therapeutics granted a total of 300,000 stock options and 300,000 restricted stock units (RSUs) to two new employees on March 26, 2026, aimed at attracting top talent and strengthening the team.
- Option Details: The options have a 10-year term with an exercise price of $0.243 per share, reflecting the fair market value on the grant date, and will vest over four years, with 25% vesting on the first anniversary and 1/36 vesting monthly thereafter.
- RSU Vesting Schedule: Each RSU represents a contingent right to one share of common stock, vesting over three years with 1/3 vesting on the first anniversary and the remainder vesting ratably over the next eight quarters, contingent on continued service with the company.
- Compliance Approval: The awards were approved by the Compensation Committee of the board, ensuring compliance with Nasdaq Rule 5635(c)(4), which reinforces the effectiveness of the inducement measures and strengthens the company's position in the industry.
See More
