Radiopharmaceutical Production Technician 2
About the job
- Typically requires 2-4 years of relevant experience in pharmaceutical, radiopharmaceutical, or other regulated current Good Manufacturing Practice manufacturing environments, or successful completion of Technician I level responsibilities at Perspective Therapeutics.
- Experience with Microsoft Office Suite.
- Demonstrated ability to understand and apply radiopharmaceutical production processes in a regulated current Good Manufacturing Practice environment.
- Ability to identify process or documentation issues, apply established troubleshooting approaches, and escalate non-routine issues appropriately.
- Ability to properly don and wear required cleanroom garments and personal protective equipment in compliance with safety and regulatory standards.
- Ability to perform physically active job duties, including standing for extended periods and performing bending, stooping, crouching, kneeling, pushing, pulling, and reaching, with or without reasonable accommodation.
- May be required to lift or move materials weighing up to approximately 50 pounds, with team lifting and/or mechanical assistance, in accordance with safety procedures.
- Flexibility to work varying shifts, including overnight and weekends, and outside regular work hours as business needs require.
- Must be willing to work in a facility with radioactive, corrosive, flammable, and toxic materials and participate in required safety programs.
- Work is performed in ISO-class environments requiring adherence to gowning and contamination-control procedures in addition to personal protective equipment.
- Willingness to complete safety training within allotted timeframes and work in a team-based environment.
- Perform manufacturing activities in an aseptic environment, including donning required cleanroom garments and personal protective equipment, performing aseptic manipulations with environmental and personnel monitoring, executing batch record calculations, maintaining accurate documentation, and resolving routine documentation discrepancies in compliance with current Good Manufacturing Practice guidelines and standard operating procedures.
- Support radiopharmaceutical production readiness through material kitting, solution preparation, line clearance, and manual cleaning of classified manufacturing areas used for sterile production.
- Provide day-to-day guidance and on-the-job training to Technician I employees on standard operating procedures, Good Manufacturing Practice practices, and safety requirements, as assigned.
- Identify and assist in resolving equipment, process, and documentation issues while documenting and escalating issues as appropriate.
- Receive radioactive materials and prepare radioactive packages for distribution in accordance with applicable regulations and standard operating procedures.
- Prepare radioactive calibration standards to support equipment setup and operation.
- Perform peer checks or verifications required by standard operating procedures, ensuring accuracy and compliance with current Good Manufacturing Practice and safety requirements.
- Adhere to As Low As Reasonably Achievable principles and Nuclear Regulatory Commission guidelines when handling radioactive materials.
- Assist with deviation investigations, change controls, and inspection readiness activities by providing documentation, data, and subject-matter input under Production or Quality leadership guidance.
- Provide input to production planning and scheduling activities as requested based on hands-on production experience.
- Bachelor's degree in a scientific discipline such as Chemistry, Biochemistry, Biology, or Pharmaceutical Sciences.
- Aseptic processing and technique experience.
- Additional certifications in radiopharmaceuticals or Good Manufacturing Practice.
About the company
Perspective Therapeutics develops targeted alpha-particle radiopharmaceuticals for cancer, using Lead-212 attached to tumor-targeting peptides and a matching Lead-203 imaging companion for patient selection. The therapy delivers lethal radiation directly to cancer cells while limiting exposure to healthy tissue. It differentiates itself by building an in-house, vertically integrated development and manufacturing platform and a planned network of isotope facilities, plus strategic partnerships to fund and co-develop programs. The goal is to bring precise isotope-based cancer therapies to patients and advance these therapies toward commercialization.
Company Size
51-200
Company Stage
IPO
Headquarters
Seattle, Washington
Founded
1998
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Simplify's Take
What believers are saying
- October 2026 ESMO and SITC acceptances keep VMT-α-NET and VMT01 visible.
- European Commission orphan designation for VMT-α-NET strengthens regulatory and commercial positioning.
- Cash of $236.9 million at June 30, 2026 funds operations into late 2027.
What critics are saying
- February 2026 raised $175 million through 46 million shares and warrants, diluting holders.
- VMT01 still treated only 27 patients; two responses in 3.0 mCi monotherapy.
- Any late-2026 data miss, FDA delay, or manufacturing failure kills the pipeline.
What makes Perspective Therapeutics unique
- Pb-212 theranostics pair imaging and therapy across NET, melanoma, and FAP tumors.
- Vertical generator-based manufacturing gives Perspective control over short-lived isotopes and finished-dose supply.
- Merck signed a September 2026 PSV359-Keytruda collaboration, validating the platform.
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Benefits
Flexible Work Hours
Growth & Insights and Company News
6 month growth
-1%1 year growth
0%2 year growth
4%Perspective Therapeutics announces acceptance of [212pb]vmt-α-net data for presentation at the NANETS 2026 Multidisciplinary NET Medical Symposium. SEATTLE, Oct. 07, 2026 (GLOBE NEWSWIRE) - Perspective Therapeutics, Inc. ("Perspective," the "Company," "we," "us," and "our") (NYSE AMERICAN: CATX), a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body, today announced that data from the Company's [[212]Pb]VMT-α-NET program have been accepted for presentation at the NANETS 2026 Multidisciplinary NET Medical Symposium taking place November 5 to 7, 2026, in Las Vegas, Nevada. | Presenter | Abstract Title | Presentation Details | | Thorvardur Halfdanarson, MD, Mayo Clinic Rochester | Cohort level safety and efficacy results for [[212] Pb]VMT-α-NET in advanced somatostatin receptor subtype 2 (SSTR2+)-expressing neuroendocrine tumors (NETs): Cohorts 1-3 | Abstract Number: 36595 Presentation type: Oral presentation Session Name: Featured Abstracts I: Evolving Therapies, Risks, and Outcomes in NETs Date: November 5, 2026 Time: 4:10 pm - 5:25 pm PST | About [[212]Pb]VMT-α-NET Perspective designed [[212] Pb]VMT-α-NET to target somatostatin receptor subtype 2 (SSTR2), and to deliver the alpha-emitting radioisotope lead-212, or 2[12]Pb, to tumor sites expressing SSTR2. The Company is conducting a multi-center, open-label, dose-escalation and dose-expansion study (clinicaltrials.gov identifier NCT05636618) of [[212] Pb]VMT-α-NET in patients with unresectable or metastatic SSTR2-positive tumors who have not received prior radiopharmaceutical therapies (RPT). Interim clinical data from the study, with a data cut-off date of April 17, 2026, were presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting in May 2026. These data included efficacy results for half of the patients in Cohort 2 and both patients in Cohort 1. Initial efficacy data for the remaining patients in Cohort 2 and patients in Cohorts 3 and 4 are pending. The Company plans to submit additional data for presentation at future medical conferences in 2026 and 2027. About Perspective Therapeutics, Inc. Perspective Therapeutics, Inc. is a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body. The Company has proprietary technology that utilizes the alpha-generating isotope [212] Pb to deliver powerful radiation specifically to cancer cells via specialized targeting moieties. The Company is also developing complementary imaging techniques that incorporate the same targeting moieties, which provides the opportunity to personalize treatment and optimize patient outcomes. This "theranostic" approach enables visualization of the specific tumor and subsequent treatment, potentially improving efficacy and minimizing toxicity. The Company is advancing a portfolio of clinical-stage programs in the U.S., including bamzireotide navoxetan (VMT-α-NET, neuroendocrine tumors), lapemelanotide zapixetar (VMT01, melanoma), and PSV359 (solid tumors). The Company is expanding its regional finished drug product candidate supply network, enabled by its proprietary [224] Ra/[212] Pb generator platform used to manufacture clinical drug product candidates, to support the delivery of patient-ready drug product candidates for clinical trials and, if approved, commercial operations. Safe Harbor Statement This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Words such as "may," "will," "should," "expect," "plan," "anticipate," "could," "intend," "target," "project," "estimate," "believe," "predict," "potential," or "continue" or the negative of these terms or other similar expressions are intended to identify forward-looking statements, though not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include statements concerning, among other things, the Company's preclinical and clinical development plans and the expected timing for the release of additional data from its clinical programs; the Company's beliefs that its product candidates address certain unmet medical needs; the Company's expectations regarding regulatory pathways for its product candidates; the Company's expectations regarding its interactions with regulatory agencies and the expected timing thereof; the Company's regional distribution and manufacturing capabilities; and other statements that are not historical fact. The Company may not actually achieve the plans, intentions, or expectations disclosed in the forward-looking statements, and you should not place undue reliance on the forward-looking statements. These forward-looking statements involve risks and uncertainties that could cause the Company's actual results to differ materially from the results described in or implied by the forward-looking statements. Known risk factors include that the Company's clinical trials may be more costly or take longer to complete than anticipated, or may never be completed, or may not generate results that warrant future development of the tested product candidate; the Company may elect to change its strategy regarding its product candidates and clinical development activities; economic and market conditions may worsen; and risks related to the sufficiency of the Company's cash resources for its future operating expenses and capital expenditures. A more complete discussion of the risks and uncertainties facing the Company appears under the heading "Risk Factors" in the Company's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (the "SEC"), in the Company's other filings with the SEC, and in the Company's future reports to be filed with the SEC and available at www.sec.gov. Forward-looking statements contained in this news release are made as of this date. Unless required to do so by law, we undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise. Media and Investor Relations Contacts:
Perspective Therapeutics announces acceptance of [212pb]vmt01 data for presentation at SITC 2026. SEATTLE, Oct. 02, 2026 (GLOBE NEWSWIRE) - Perspective Therapeutics, Inc. ("Perspective," the "Company," "we," "us," and "our") (NYSE AMERICAN: CATX), a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body, today announced that data from the Company's lapemelanotide zapixetar (also known as [[212]Pb]VMT01) program have been accepted for presentation at the Society for Immunotherapy of Cancer (SITC) 41st Annual Meeting & Pre-Conference Programs taking place November 4 to 8, 2026, in Phoenix, Arizona. SITC plans to release further details for regular abstracts on November 3, 2026. | Presenting Author | Abstract Title | Presentation Details | | Matthew Block, Department of Oncology, Mayo Clinic | A phase I/IIa trial of [[212] Pb]VMT01 MC1R-targeted alpha-particle mono- and combination-therapy with nivolumab in participants with previously treated unresectable or metastatic melanoma | Abstract Number: 571 Presentation type: Poster presentation Date: Friday, Nov. 6, 2026 Location: PCC-North Building-Lower Level-Exhibition Halls 4-5-6 | About [[212]Pb]VMT-01 Perspective designed [[212] Pb]VMT01 to target and deliver [212] Pb to metastatic melanoma tumor sites expressing MC1R, a protein that can be overexpressed in metastatic melanoma tumors.[1] The Company is conducting a multi-center, open-label dose escalation, dose expansion study (clinicaltrials.gov identifier NCT05655312) in patients with histologically confirmed melanoma and MC1R-positive imaging scans. Interim analysis with a data cut-off date of March 25, 2026 was presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting in May 2026. Highlights from the ASCO analysis included the following: * Patients were heavily pre-treated prior to entering trial with a median of 4 prior lines of systemic therapy (including prior checkpoint inhibitors) * One new response was observed early in the 3.0 mCi monotherapy cohort, in addition to a previously reported response, for a total of two responders out of seven treated patients * Six patients (86%) experienced stable disease or partial response out of the seven patients in the 3.0 mCi monotherapy cohort; four patients completed all three treatments with 24 weeks or more of follow-up since their first treatment, and two remained on treatment and in study * [[212]Pb]VMT01 was well-tolerated with no dose limiting toxicities (DLTs), no discontinuations due to adverse events, and no Grade 4 or Grade 5 treatment emergent adverse events (TEAEs) * Eight (30%) patients out of a total of 27 patients treated experienced Grade 3 TEAEs About Perspective Therapeutics, Inc. Perspective Therapeutics, Inc. is a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body. The Company has proprietary technology that utilizes the alpha-generating isotope [212] Pb to deliver powerful radiation specifically to cancer cells via specialized targeting moieties. The Company is also developing complementary imaging techniques that incorporate the same targeting moieties, which provides the opportunity to personalize treatment and optimize patient outcomes. This "theranostic" approach enables visualization of the specific tumor and subsequent treatment, potentially improving efficacy and minimizing toxicity. The Company is advancing a portfolio of clinical-stage programs in the U.S., including bamzireotide navoxetan (VMT-α-NET, neuroendocrine tumors), lapemelanotide zapixetar (VMT01, melanoma), and PSV359 (solid tumors). The Company is expanding its regional finished drug product candidate supply network, enabled by its proprietary [224] Ra/[212] Pb generator platform used to manufacture clinical drug product candidates, to support the delivery of patient-ready drug product candidates for clinical trials and, if approved, commercial operations. Safe Harbor Statement This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Words such as "may," "will," "should," "expect," "plan," "anticipate," "could," "intend," "target," "project," "estimate," "believe," "predict," "potential," or "continue" or the negative of these terms or other similar expressions are intended to identify forward-looking statements, though not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include statements concerning, among other things, the Company's clinical development plans and the expected timing for the release of additional data from its clinical programs; the Company's regional distribution and manufacturing capabilities; and other statements that are not historical fact. The Company may not actually achieve the plans, intentions, or expectations disclosed in the forward-looking statements, and you should not place undue reliance on the forward-looking statements. These forward-looking statements involve risks and uncertainties that could cause the Company's actual results to differ materially from the results described in or implied by the forward-looking statements. Known risk factors include that the Company's preclinical development plans and clinical trials may be more costly or take longer to complete than anticipated, or may never be completed, or may not generate results that warrant future development of the tested product candidate; the Company may elect to change its strategy regarding its product candidates and development activities; economic and market conditions may worsen; regulatory agencies may issue decisions that negatively impact the Company's product candidates and clinical development plans; and risks related to the sufficiency of the Company's cash resources for its future operating expenses and capital expenditures. A more complete discussion of the risks and uncertainties facing the Company appears under the heading "Risk Factors" in the Company's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (the "SEC"), in the Company's other filings with the SEC, and in the Company's future reports to be filed with the SEC and available at www.sec.gov. Forward-looking statements contained in this news release are made as of this date. Unless required to do so by law, we undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise. Media and Investor Relations Contacts: [1] Su DG, Djureinovic D, Schoenfeld D, et al. Melanocortin-1 Receptor Expression as a Marker of Progression in Melanoma. JCO Precis Oncol. 2024;8:e2300702. doi:10.1200/PO.23.00702.
Perspective Therapeutics announces acceptance of vmt-α-net data for presentation at the 38th EORTC-NCI-AACR Symposium 2026. SEATTLE, Sept. 11, 2026 (GLOBE NEWSWIRE) - Perspective Therapeutics, Inc. ("Perspective," the "Company," "we," "us," and "our") (NYSE AMERICAN: CATX), a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body, today announced that updated data on the Company's [[212] Pb]VMT-α-NET program have been accepted for presentation as detailed below at the 38th EORTC-NCI-AACR (ENA) Symposium 2026 on Molecular Targets and Cancer Therapeutics taking place November 18 to 20, 2026 in Barcelona, Spain. The conference plans to release further details for abstracts on November 4, 2026. | Presenter | Abstract Title | Presentation Details | | Vikas Prasad, Washington University School of Medicine | Cohort level safety and efficacy results for [[212] Pb]VMT-α-NET in advanced somatostatin receptor subtype 2 (SSTR2+)-expressing neuroendocrine tumors (NETs): Cohorts 1-3 | Abstract Number: 334 Session Type: Poster session Session Title: New drugs Session Date: November 20, 2026 Session Time: 9:00am - 3:00pm CET / 3:00am - 9:00 am EST | About [[212]Pb]VMT-α-NET Perspective designed [[212] Pb]VMT-α-NET to target somatostatin receptor subtype 2 (SSTR2), and to deliver the alpha-emitting radioisotope lead-212, or 2[12]Pb, to tumor sites expressing SSTR2. The Company is conducting a multi-center, open-label, dose-escalation and dose-expansion study (clinicaltrials.gov identifier NCT05636618) of [[212] Pb]VMT-α-NET in patients with unresectable or metastatic SSTR2-positive tumors who have not received prior radiopharmaceutical therapies (RPT). Interim clinical data from the study, with a data cut-off date of April 17, 2026, were presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting in May 2026. These data included efficacy results for half of the patients in Cohort 2 and both patients in Cohort 1. Initial efficacy data for the remaining patients in Cohort 2 and patients in Cohorts 3 and 4 are pending. The Company plans to submit additional data for presentation at future medical conferences in 2026 and 2027. About Perspective Therapeutics, Inc. Perspective Therapeutics, Inc. is a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body. The Company has proprietary technology that utilizes the alpha-generating isotope [212] Pb to deliver powerful radiation specifically to cancer cells via specialized targeting moieties. The Company is also developing complementary imaging techniques that incorporate the same targeting moieties, which provides the opportunity to personalize treatment and optimize patient outcomes. This "theranostic" approach enables visualization of the specific tumor and subsequent treatment, potentially improving efficacy and minimizing toxicity. The Company is advancing a portfolio of clinical-stage programs in the U.S., including bamzireotide navoxetan (VMT-α-NET, neuroendocrine tumors), lapemelanotide zapixetar (VMT01, melanoma), and PSV359 (solid tumors). The Company is expanding its regional finished drug product candidate supply network, enabled by its proprietary [224] Ra/[212] Pb generator platform used to manufacture clinical drug product candidates, to support the delivery of patient-ready drug product candidates for clinical trials and, if approved, commercial operations. Safe Harbor Statement This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Words such as "may," "will," "should," "expect," "plan," "anticipate," "could," "intend," "target," "project," "estimate," "believe," "predict," "potential," or "continue" or the negative of these terms or other similar expressions are intended to identify forward-looking statements, though not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include statements concerning, among other things, the Company's preclinical and clinical development plans and the expected timing for the release of additional data from its clinical programs; the Company's beliefs that its product candidates address certain unmet medical needs; the Company's regional distribution and manufacturing capabilities; and other statements that are not historical fact. The Company may not actually achieve the plans, intentions, or expectations disclosed in the forward-looking statements, and you should not place undue reliance on the forward-looking statements. These forward-looking statements involve risks and uncertainties that could cause the Company's actual results to differ materially from the results described in or implied by the forward-looking statements. Known risk factors include that the Company's clinical trials may be more costly or take longer to complete than anticipated, or may never be completed, or may not generate results that warrant future development of the tested product candidate; the Company may elect to change its strategy regarding its product candidates and clinical development activities; economic and market conditions may worsen; and risks related to the sufficiency of the Company's cash resources for its future operating expenses and capital expenditures. A more complete discussion of the risks and uncertainties facing the Company appears under the heading "Risk Factors" in the Company's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (the "SEC"), in the Company's other filings with the SEC, and in the Company's future reports to be filed with the SEC and available at www.sec.gov. Forward-looking statements contained in this news release are made as of this date. Unless required to do so by law, we undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise. Media and Investor Relations Contacts:
Bank of America lowers Perspective Therapeutics (NYSEAMERICAN:CATX) price target to $5.00. August 14, 2026 Key points. * Bank of America lowered Perspective Therapeutics' price target from $6.00 to $5.00 while maintaining a neutral rating; the revised target implies approximately 57% upside from the prior close. * Analyst sentiment remains broadly positive, with eight Buy ratings and one Hold rating producing a "Moderate Buy" consensus and an average price target of $11.56. * Perspective Therapeutics reported a quarterly loss of $0.22 per share, better than the expected $0.25 loss, but revenue was just $0.08 million and the company continues to post substantial losses as it advances its early-stage cancer therapies. * Five stocks we like better than Perspective Therapeutics. Perspective Therapeutics (NYSEAMERICAN:CATX - Get Free Report) had its price target reduced by equities researchers at Bank of America from $6.00 to $5.00 in a report released on Friday,Benzinga reports. The firm presently has a "neutral" rating on the stock. Bank of America's price objective would suggest a potential upside of 56.99% from the company's previous close. Other equities research analysts also recently issued research reports about the stock. BTIG Research reissued a "buy" rating on shares of Perspective Therapeutics in a research report on Friday, July 24th. Wedbush reaffirmed an "outperform" rating and set a $11.00 price target on shares of Perspective Therapeutics in a report on Tuesday, May 5th. Finally, Piper Sandler reduced their price objective on Perspective Therapeutics from $16.00 to $14.00 and set an "overweight" rating for the company in a report on Tuesday. Eight research analysts have rated the stock with a Buy rating and one has assigned a Hold rating to the company. According to data from MarketBeat, Perspective Therapeutics currently has an average rating of "Moderate Buy" and an average target price of $11.56. Perspective Therapeutics Stock up 2.7%. CATX stock traded up $0.09 on Friday, reaching $3.19. 588,403 shares of the company traded hands, compared to its average volume of 2,325,881. The firm has a fifty day simple moving average of $3.08 and a 200-day simple moving average of $3.94. Perspective Therapeutics has a one year low of $1.96 and a one year high of $6.16. Perspective Therapeutics (NYSEAMERICAN:CATX - Get Free Report) last announced its quarterly earnings results on Monday, August 10th. The company reported ($0.22) earnings per share (EPS) for the quarter, topping analysts' consensus estimates of ($0.25) by $0.03. The company had revenue of $0.08 million for the quarter, compared to analysts' expectations of $0.09 million. Perspective Therapeutics had a negative net margin of 28,467.97% and a negative return on equity of 44.22%. On average, research analysts forecast that Perspective Therapeutics will post -1.07 EPS for the current fiscal year. Hedge funds weigh in on Perspective Therapeutics. Institutional investors and hedge funds have recently modified their holdings of the company. Portland Investment Counsel Inc. purchased a new stake in Perspective Therapeutics during the second quarter valued at $852,000. Bank of New York Mellon Corp bought a new stake in shares of Perspective Therapeutics during the 2nd quarter valued at about $1,015,000. Taylor & Morgan Wealth Management LLC grew its stake in shares of Perspective Therapeutics by 127.6% during the 2nd quarter. Taylor & Morgan Wealth Management LLC now owns 66,000 shares of the company's stock valued at $225,000 after purchasing an additional 37,000 shares during the period. Seven Fleet Capital Management LP purchased a new stake in shares of Perspective Therapeutics during the 1st quarter valued at about $1,581,000. Finally, Avidity Partners Management LP increased its position in shares of Perspective Therapeutics by 88.4% during the 1st quarter. Avidity Partners Management LP now owns 6,049,999 shares of the company's stock valued at $25,228,000 after purchasing an additional 2,839,266 shares during the last quarter. 54.66% of the stock is currently owned by hedge funds and other institutional investors. Key headlines impacting Perspective Therapeutics. Here are the key news stories impacting Perspective Therapeutics this week: * Positive Sentiment: Brookline Capital Markets raised its 2026 loss estimates: Analyst K. Dolliver now expects a loss of $0.25 per share for the third quarter, $0.26 for the fourth quarter and $0.99 for full-year 2026, compared with previous estimates of $0.32, $0.36 and $1.23, respectively. Smaller projected losses may signal improved expectations for operating performance and could support CATX shares. * Neutral Sentiment: Losses are still expected through 2027. Brookline forecasts quarterly losses of $0.26, $0.27, $0.30 and $0.32 for the first four quarters of 2027, totaling a projected $1.14 loss for the year. The estimates highlight that Perspective Therapeutics remains an early-stage, loss-making biotechnology company, with future results dependent on clinical and commercial progress. * Negative Sentiment: Piper Sandler lowered its expectations for the stock price, indicating a less favorable near-term view of CATX's valuation. The available report does not provide the revised target or the specific reasons for the change. Piper Sandler Has Lowered Expectations for Perspective Therapeutics Stock Price About Perspective Therapeutics. Perspective Therapeutics, Inc, together with its subsidiaries, develops precision-targeted alpha therapies (TAT) for oncology that treats cancer patients across multiple tumor types comprising metastatic disease. The company discovers, designs, and develop its initial programs candidates consists of VMT-a-NET, that is currently in Phase 1/2a clinical trials for patients with unresectable or metastatic somatostatin receptor type 2 (SSTR2) expressing tumors that have not previously received peptide-targeted radiopharmaceutical therapy, such as Lutathera, a beta-emitting therapy; and VMT01, which is currently in Phase 1/2a clinical trials for second-line or later treatment of patients with progressive melanocortin 1 receptor (MC1R) positive metastatic melanoma. This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected]. Continue following MarketBeat Before you consider Perspective Therapeutics, you'll want to hear this. 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Perspective Therapeutics announces acceptance of VMT-α-NET data for oral presentation at the ESMO Congress 2026. GlobeNewswire | Perspective Therapeutics, Inc. Today at 9:22am PDT SEATTLE, July 17, 2026 (GLOBE NEWSWIRE) - Perspective Therapeutics, Inc. ("Perspective," the "Company," "we," "us," and "our") (NYSE AMERICAN: CATX), a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body, today announced that updated data on the Company's [[212] Pb]VMT-α-NET program have been accepted for presentation as detailed below at the European Society of Medical Oncology (ESMO) Congress 2026 taking place October 23 to 27, 2026 in Madrid, Spain. ESMO plans to release further details for regular abstracts on October 19, 2026. | Presenter | Abstract Title | Presentation Details | | Thorvardur Halfdanarson, Mayo Clinic Comprehensive Cancer Center | Cohort level safety and efficacy results for [[212] Pb]VMT-α-NET in advanced somatostatin receptor subtype 2 (SSTR2+)-expressing neuroendocrine tumors (NETs): Cohorts 1-3 | Abstract Number: 2396RO Session Type: Rapid Oral presentation Session Title: Rapid oral: NETs and endocrine tumours Session Date: October 23, 2026 Session Time: 4:15 - 5:45pm CEST / 10:15 - 11:45am EDT Presentation Time: 4:25 - 4:30pm CEST / 10:25 - 10:30am EDT | About [[212]Pb]VMT-α-NET Perspective designed [[212] Pb]VMT-α-NET to target somatostatin receptor subtype 2 (SSTR2), and to deliver the alpha-emitting radioisotope lead-212, or 2[12]Pb, to tumor sites expressing SSTR2. The Company is conducting a multi-center, open-label, dose-escalation and dose-expansion study (clinicaltrials.gov identifier NCT05636618) of [[212] Pb]VMT-α-NET in patients with unresectable or metastatic SSTR2-positive tumors who have not received prior radiopharmaceutical therapies (RPT). Interim clinical data from the study, with a data cut-off date of April 17, 2026, were presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting in May 2026. These data included efficacy results for half of the patients in Cohort 2 and both patients in Cohort 1. Initial efficacy data for the remaining patients in Cohort 2 and patients in Cohorts 3 and 4 are pending. The Company plans to submit additional data for presentation at future medical conferences in 2026 and 2027. About Perspective Therapeutics, Inc. Perspective Therapeutics, Inc. is a radiopharmaceutical development company pioneering advanced treatments for cancers throughout the body. The Company has proprietary technology that utilizes the alpha-generating isotope [212] Pb to deliver powerful radiation specifically to cancer cells via specialized targeting moieties. The Company is also developing complementary imaging techniques that incorporate the same targeting moieties, which provides the opportunity to personalize treatment and optimize patient outcomes. This "theranostic" approach enables visualization of the specific tumor and subsequent treatment, potentially improving efficacy and minimizing toxicity. The Company is advancing a portfolio of clinical-stage programs in the U.S., including VMT-α-NET (neuroendocrine tumors), VMT01 (melanoma), and PSV359 (solid tumors). The Company is expanding its regional finished drug product candidate supply network, enabled by its proprietary [224] Ra/[212] Pb generator platform used to manufacture clinical drug product candidates, to support the delivery of patient-ready drug product candidates for clinical trials and, if approved, commercial operations. Safe Harbor Statement This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Words such as "may," "will," "should," "expect," "plan," "anticipate," "could," "intend," "target," "project," "estimate," "believe," "predict," "potential," or "continue" or the negative of these terms or other similar expressions are intended to identify forward-looking statements, though not all forward-looking statements contain these identifying words. Forward-looking statements in this press release include statements concerning, among other things, the Company's preclinical and clinical development plans and the expected timing for the release of additional data from its clinical programs; the Company's beliefs that its product candidates address certain unmet medical needs; the Company's expectations regarding regulatory pathways for its product candidates; the Company's expectations regarding its interactions with regulatory agencies and the expected timing thereof; the Company's regional distribution and manufacturing capabilities; and other statements that are not historical fact. The Company may not actually achieve the plans, intentions, or expectations disclosed in the forward-looking statements, and you should not place undue reliance on the forward-looking statements. These forward-looking statements involve risks and uncertainties that could cause the Company's actual results to differ materially from the results described in or implied by the forward-looking statements. Known risk factors include that the Company's clinical trials may be more costly or take longer to complete than anticipated, or may never be completed, or may not generate results that warrant future development of the tested product candidate; the Company may elect to change its strategy regarding its product candidates and clinical development activities; economic and market conditions may worsen; and risks related to the sufficiency of the Company's cash resources for its future operating expenses and capital expenditures. A more complete discussion of the risks and uncertainties facing the Company appears under the heading "Risk Factors" in the Company's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (the "SEC"), in the Company's other filings with the SEC, and in the Company's future reports to be filed with the SEC and available at www.sec.gov. Forward-looking statements contained in this news release are made as of this date. Unless required to do so by law, Newberggraphic undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise. Media and Investor Relations Contacts: This is a paid placement. For further inquiries, please contact GlobeNewswire directly.