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Purple Biotech Reports Positive New Preclinical Data Demonstrating Multi-Arm Anti-Tumor Activity Across Two CAPTN-3 Tri-Specific Antibodies at ESMO Immuno-Oncology Congress 2025
Globenewswire· 2025-12-11 12:00
Data demonstrates the significant and sustained tumor regression achieved by the CAPTN-3 platform across two distinct tri-specific antibodies, IM1240 and IM1305, targeting different tumor antigens Transcriptomic analysis across ~11,000 TCGA samples shows NKG2A expression is strongly associated with tumor expression of 5T4 or TROP2, supporting inclusion of the NKG2A arm in CAPTN-3 designs NKG2A arm significantly contributes to IM1240 anti-cancer immune activity in PD1-resistant patient-derived explants REHOV ...
Purple Biotech to Present New Preclinical Data from its CAPTN-3 Tri-Specific Antibody Platform at the European Society of Medical Oncology Immuno-Oncology (ESMO-IO) 2025 Annual Congress
Globenewswire· 2025-12-04 12:00
New data showcase the versatility and anti-tumor activity of the CAPTN-3 platform and its unique multi-arm design in treatment-resistant cancers     REHOVOT, Israel, Dec. 04, 2025 (GLOBE NEWSWIRE) -- Purple Biotech Ltd. (“Purple Biotech” or “the Company”) (NASDAQ/TASE: PPBT), a clinical-stage company developing first-in-class therapies that seek to overcome tumor immune evasion and drug resistance, today announced that it will present new preclinical data from its CAPTN-3 platform of conditionally activated ...
Purple Biotech Reports Third Quarter 2025 Financial Results and Provides Business Update
Globenewswire· 2025-11-14 13:00
Core Insights - Purple Biotech Ltd. has initiated the development of a second tri-specific antibody, IM1305, targeting TROP2, and achieved a manufacturing milestone for its first tri-specific antibody, IM1240, which targets 5T4 [1][4] - The company reported a cash position of $10.5 million as of September 30, 2025, with an expected cash runway into the first half of 2027, supporting the development of its CAPTN-3 technology platform [1][10] Financial Performance - Research and Development Expenses for the three months ended September 30, 2025, were $0.6 million, a decrease of 56.4% from $1.3 million in the same period of 2024, primarily due to reduced costs associated with the CM24 Phase 2 study [5] - General and Administrative Expenses remained consistent at $0.8 million for the three months ended September 30, 2025, compared to the same period in 2024 [6] - The Operating Loss for the three months ended September 30, 2025, was $1.4 million, a decrease of 35.8% from $2.1 million in the same period of 2024 [6] - The Net Loss for the three months ended September 30, 2025, was $1.3 million, or $0.29 per basic and diluted ADS, compared to a net loss of $0.7 million, or $0.39 per basic and diluted ADS, in the same period of 2024 [9] Clinical and Corporate Developments - The company plans to conduct non-GLP and GLP toxicology studies, submit an Investigational New Drug application (IND), and initiate a Phase 1 study for IM1240 in 2026 [2] - IM1240 has demonstrated tumor cell death in patient-derived, treatment-resistant head and neck biopsies, advancing toward first-in-human clinical trials [4] - The CM24 Phase 2 study will utilize identified biomarkers for patient selection in the upcoming Phase 2b study, which is subject to partnering [4] Patent and Intellectual Property - Purple Biotech received an intention to grant a European patent covering NT219 combinations with immunotherapies or MEK inhibitors to overcome tumor resistance [3][5]
Purple Biotech Announces Receipt of Nasdaq Minimum Bid Price Notification
Globenewswire· 2025-10-20 20:00
Core Points - Purple Biotech Ltd. has received a notification from Nasdaq regarding non-compliance with the minimum bid price requirement, as the closing bid price for its American Depositary Shares (ADSs) has been below $1.00 for 30 consecutive trading days [1] - The company has a 180-day period until April 14, 2026, to regain compliance by achieving a closing bid price of $1.00 or more for at least ten consecutive business days [2] - The notification does not affect the company's current Nasdaq listing or trading of its ADSs, which will continue under the symbol "PPBT" [3] Compliance and Remediation - If compliance is not regained by April 14, 2026, the company may be eligible for an additional 180 days to cure the deficiency, provided it meets other listing requirements [4] - The company intends to monitor its ADS closing bid price and may consider options to regain compliance, including potentially changing the ADS to ordinary shares ratio [5] Company Overview - Purple Biotech is a clinical-stage company focused on developing first-in-class therapies to combat tumor immune evasion and drug resistance, with a pipeline that includes CAPTN-3, CM24, and NT219 [6] - CAPTN-3 is a preclinical platform utilizing tri-specific antibodies to enhance immune response within the tumor microenvironment, while CM24 is a humanized monoclonal antibody targeting CEACAM1 to block tumor immune evasion [6][7] - NT219 is a novel small molecule that targets IRS1/2 and STAT3, showing anti-tumor activity in combination with cetuximab in clinical studies [7]
Kura Oncology (NasdaqGS:KURA) Update / Briefing Transcript
2025-09-16 21:32
Kura Oncology Conference Call Summary Company Overview - **Company**: Kura Oncology (NasdaqGS: KURA) - **Focus**: Development of targeted therapies for cancer treatment, particularly through the use of Farnesyl Transferase Inhibitors (FTIs) and menin inhibitors. Key Points Industry and Product Pipeline - Kura is well-positioned to build on the success of Ziftomenib, currently under FDA review for NPM1-mutant relapsed/refractory Acute Myeloid Leukemia (AML) [3][4] - The menin inhibitor class could represent a market opportunity of $5 to $10 billion, with Kura aiming to capture a significant share [3] - The company is advancing its FTI program, specifically KO-2806 (Darlifarnib), which is designed to overcome drug resistance in various cancers [12][26] Preclinical Data and Mechanism of Action - KO-2806 has shown improved potency and reduced dosing requirements compared to its predecessor, Tipifarnib, making it suitable for combination therapies [12][13] - The FTI program targets Rheb, a protein involved in mTOR signaling, which is crucial for addressing resistance to multiple targeted therapies [8][18] - Preclinical studies indicate that KO-2806 enhances the efficacy of various therapies, including PI3K inhibitors, KRAS inhibitors, and anti-angiogenic TKIs, across multiple cancer types [26][27] Clinical Development Strategy - Kura is conducting several clinical trials, including: - A dose escalation trial for KO-2806 in RAS mutant tumors [30] - A combination trial of KO-2806 with Cabozantinib in renal cell carcinoma [31] - A trial combining Tipifarnib with Alpelisib in PIK3CA mutant head and neck squamous cell carcinoma [32] - The company anticipates presenting data at the upcoming ESMO meeting, focusing on safety, tolerability, and efficacy of these combinations [27][30] Market Opportunity - Kura estimates a patient population of over 200,000 annually in the U.S. for potential applications of FTIs in combination with other targeted therapies [34] - The company is optimistic about the commercial launch of Ziftomenib and ongoing studies, including the KOMET-001 phase three studies [35][36] Financial Position - Kura reported $630.7 million in cash and cash equivalents, with anticipated milestone payments of $375 million expected by year-end [36] Future Directions - Kura is exploring various clinical collaborations and partnerships to enhance the development of KO-2806 and its applications across different cancer types [60][61] - The company aims to demonstrate the additive efficacy of KO-2806 in combination therapies, addressing the challenge of proving its value alongside established agents [81] Additional Insights - The call highlighted the importance of demonstrating single-agent activity for future development, although Kura is currently focused on combination therapies [52] - The potential for KO-2806 to overcome resistance mechanisms associated with other combination regimens was also discussed, indicating a broad applicability of the FTI approach [81] This summary encapsulates the key points from the Kura Oncology conference call, focusing on the company's strategic direction, product pipeline, and market opportunities.
Kura Oncology Highlights Preclinical Data Demonstrating Potential of Farnesyl Transferase Inhibitors to Overcome Drug Resistance in Combination with Key Targeted Therapies Across Multiple Tumor Types
Globenewswire· 2025-09-16 20:01
Core Insights - Kura Oncology is showcasing the potential of KO-2806 (darlifarnib) in combination with various targeted therapies to enhance anti-tumor activity and address resistance mechanisms in cancer treatment [1][2][4] Group 1: KO-2806 Development and Clinical Data - KO-2806 is a next-generation farnesyl transferase inhibitor (FTI) designed for superior potency and pharmacokinetics compared to first-generation candidates [4] - Preliminary clinical data for KO-2806 will be presented at the ESMO Congress 2025 in October [1][5] - The company is conducting ongoing Phase 1 trials for KO-2806, with a focus on its combination with standard-of-care agents [4] Group 2: Mechanisms of Action and Preclinical Findings - KO-2806 has shown robust preclinical activity by suppressing mTOR signaling, enhancing the efficacy of antiangiogenic TKIs, PI3Kα inhibitors, and KRAS inhibitors [4] - The preclinical studies indicate that KO-2806 can re-sensitize tumors in non-small cell lung cancer (NSCLC) and colorectal cancer (CRC) models to KRAS inhibitors [4] - The findings suggest broad applicability across multiple cancer types, potentially impacting over 200,000 new patients annually in the U.S. [4] Group 3: Future Events and Presentations - Kura plans a second analyst/investor event on October 18, 2025, to review clinical data from the ESMO Congress presentations [5] - The company emphasizes the importance of innovative combination therapies to overcome resistance in cancer treatment [2][4]
Purple Biotech Receives Intention to Grant a European Patent Covering NT219 Combinations with Immunotherapies or MEK Inhibitors to Overcome Tumor Resistance
Globenewswire· 2025-09-10 12:00
Core Viewpoint - Purple Biotech Ltd. is advancing its clinical-stage therapies, particularly NT219, which targets tumor immune evasion and drug resistance, and has received an intention to grant a European Patent for its combination therapies [1][2][3] Company Overview - Purple Biotech is a clinical-stage company focused on developing first-in-class therapies to combat tumor immune evasion and drug resistance, with a pipeline that includes NT219, CAPTN-3, and CM24 [4] - The company is headquartered in Rehovot, Israel, and is publicly traded on NASDAQ and TASE under the ticker PPBT [4] Patent and Intellectual Property - The European Patent Office intends to grant a patent for NT219 combinations with leading immunotherapies, which could provide broad protection until 2036 [2] - The patent covers combinations of NT219 with various immunotherapies and chemotherapies, aimed at enhancing treatment sensitivity for resistant tumors [2] Clinical Development - A Phase 2 study for NT219 in combination with immunotherapy is underway, specifically targeting squamous cell carcinoma of the head and neck [3][5] - The study evaluates NT219 with pembrolizumab and cetuximab, building on previous Phase 1 results that showed anti-tumor activity [3][5] - Preclinical data supports the synergistic effects of NT219 with immunotherapy, indicating a shift in the tumor microenvironment from immunosuppressive to immunoreactive [3] Therapeutic Mechanism - NT219 functions as a dual inhibitor targeting IRS1/2 and STAT3, both of which are critical in drug resistance and tumor immune evasion [3][5] - The company is also developing CAPTN-3, a platform of tri-specific antibodies designed to enhance immune response within the tumor microenvironment [4]
Purple Biotech Announces Closing of Up To $18 Million Public Offering $6 million upfront with up to an additional $12 million of potential aggregate gross proceeds upon the exercise in full of short-term warrants
GlobeNewswire News Room· 2025-09-05 20:00
Core Viewpoint - Purple Biotech Ltd. has successfully closed a public offering of 5,999,999 American Depositary Shares (ADSs) at a price of $1.00 per share, with additional short-term warrants potentially raising gross proceeds of approximately $12 million if fully exercised [1][3]. Group 1: Offering Details - The public offering included 5,999,999 ADSs, each representing 200 ordinary shares, and short-term warrants to purchase up to 11,999,998 ADSs [1]. - The gross proceeds from the offering were approximately $6 million before deducting fees and expenses [3]. - The short-term warrants have an exercise price of $1.00 per ADS and are exercisable immediately, expiring twenty-four months from issuance [1][3]. Group 2: Use of Proceeds - The net proceeds from the offering will be used for the development of oncology therapeutic candidates and for general working capital and corporate purposes [3]. Group 3: Company Overview - Purple Biotech is a clinical-stage company focused on developing first-in-class therapies to overcome tumor immune evasion and drug resistance [6]. - The company's oncology pipeline includes CAPTN-3, CM24, and NT219, with CAPTN-3 being a preclinical platform of conditionally activated tri-specific antibodies [6]. - CM24 is a humanized monoclonal antibody targeting CEACAM1, and NT219 is a dual inhibitor targeting IRS1/2 and STAT3, with ongoing clinical studies demonstrating anti-tumor activity [6].
Purple Biotech Announces Pricing of Up To $18 Million Public Offering
Globenewswire· 2025-09-04 13:15
Company Overview - Purple Biotech Ltd. is a clinical-stage company focused on developing first-in-class therapies to overcome tumor immune evasion and drug resistance [6] - The company's oncology pipeline includes CAPTN-3, CM24, and NT219, with innovative mechanisms targeting various cancer indications [6][7] Public Offering Details - Purple Biotech announced a public offering of 5,999,999 American Depositary Shares (ADSs) at a price of $1.00 per share, with short-term warrants to purchase up to 11,999,998 ADSs [1][3] - The gross proceeds from the offering are expected to be approximately $6 million, with potential additional proceeds of about $12 million from the exercise of short-term warrants [3] Use of Proceeds - The net proceeds from the offering will be utilized for the development of oncology therapeutic candidates and for general working capital and corporate purposes [3] Regulatory Information - The offering is conducted under a registration statement on Form F-1, which was declared effective by the SEC on September 4, 2025 [4]
Purple Biotech to Participate in the H.C. Wainwright 27th Annual Global Investment Conference
Globenewswire· 2025-08-27 11:00
Company Overview - Purple Biotech Ltd. is a clinical-stage company focused on developing first-in-class therapies to overcome tumor immune evasion and drug resistance [3] - The company's oncology pipeline includes CAPTN-3, CM24, and NT219, which are designed to enhance immune response against tumors [3] Pipeline Details - CAPTN-3 is a preclinical platform of conditionally activated tri-specific antibodies that engage T cells and NK cells to induce a localized immune response within the tumor microenvironment [3] - CM24 is a humanized monoclonal antibody that blocks CEACAM1, a target that supports tumor immune evasion and survival [3] - NT219 is a dual inhibitor targeting IRS1/2 and STAT3, showing anti-tumor activity in combination with cetuximab for recurrent and/or metastatic squamous cell carcinoma of the head and neck [3] Recent Events - The CEO of Purple Biotech, Gil Efron, will participate in a fireside chat and 1x1 investor meetings at the H.C. Wainwright 27 Annual Global Investment Conference scheduled for September 8-10, 2025 [1][2]