– Results from Phase 1b clinical trial evaluating onvansertib + paclitaxel for metastatic triple negative breast cancer demonstrated 40% objective response rate – – The trial evaluated three doses of onvansertib in combination with paclitaxel, and objective responses were observed only at the highest dose of onvansertib – – The combination was well-tolerated and demonstrated a safe and manageable toxicity profile – SAN DIEGO, June 02, 2025 (GLOBE NEWSWIRE) -- Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinica ...

Zai Lab Limited ZLAB and NovoCure Limited NVCR revealed additional data on Saturday from the Phase 3 PANOVA-3 trial of Tumor Treating Fields (TTFields) therapy for pancreatic cancer.The data were presented at the 2025 American Society of Clinical Oncology Annual Meeting.The Phase 3 PANOVA-3 trial evaluated the use of TTFields therapy concomitantly with gemcitabine and nab-paclitaxel as a first-line treatment for unresectable, locally advanced pancreatic adenocarcinoma compared to gemcitabine and nab-paclita ...

Core Insights - BioLineRx Ltd is presenting new data from the CheMo4METPANC Phase 2 trial at the 2025 American Society of Clinical Oncology Annual Meeting, which evaluates a combination of motixafortide, cemiplimab, and standard chemotherapies for first-line pancreatic cancer [1] Group 1: Clinical Trial Results - The pilot phase of the trial showed that four out of eleven patients remained progression-free after more than one year [2] - The overall response rate (ORR) was 64% (7 out of 11), and the disease control rate (DCR) was 91% (10 out of 11), significantly higher than historical rates of 23% and 48% for gemcitabine and nab-paclitaxel [5] - The trial is the first large, multi-center, randomized study evaluating motixafortide with a PD-1 inhibitor and first-line PDAC chemotherapies, with full enrollment expected by 2027 [6] Group 2: Patient Outcomes - Two patients with metastatic pancreatic cancer (mPDAC) underwent definitive treatment, with one achieving complete resolution of liver lesions and the other showing a sustained partial response [3] - An increase in CD8+ T-cell tumor infiltration was observed across all eleven patients treated with the motixafortide combination, indicating a potential immune response [4] Group 3: Company Financials and Market Response - BioLineRx has reduced its operating expense run rate by over 70% starting January 1, 2025, due to the transfer of the APHEXDA program and the shutdown of U.S. commercial operations [7] - The company raised gross proceeds of $10 million in financing and reaffirmed its cash runway through the second half of 2026 [7] - Following these developments, Jones Trading upgraded BioLineRx from Hold to Buy with a price target of $12, and the stock price increased by 42.7% to $5.41 [8]

FDA Breakthrough Device Designation Awarded to AVIM Therapy FDA IDE Approved for Virtue SAB U.S. Pivotal Trial for Launch NEW HOPE, Pa., May 12, 2025 (GLOBE NEWSWIRE) -- Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO, “Orchestra BioMed” or the “Company”), a biomedical company accelerating high-impact technologies to patients through risk-reward sharing partnerships, today announced financial results for the first quarter ended March 31, 2025, and provided a business update highlighting continued regulatory m ...

Core Insights - Theriva Biologics announced positive topline outcomes from the VIRAGE Phase 2b clinical trial for VCN-01 in combination with standard-of-care chemotherapy for metastatic pancreatic ductal adenocarcinoma (PDAC) patients [1][3] Company Overview - Theriva Biologics is a diversified clinical-stage company focused on developing therapeutics for cancer and related diseases, with its lead product candidate being VCN-01, an oncolytic adenovirus [10][11] Clinical Trial Results - The VIRAGE trial involved 96 newly-diagnosed metastatic PDAC patients, showing that patients receiving 2 doses of VCN-01 plus chemotherapy had a median overall survival (OS) of 14.8 months compared to 11.6 months for those receiving chemotherapy alone [2] - In the primary endpoint analysis, patients treated with VCN-01 followed by chemotherapy had a median OS of 10.8 months, while those receiving only chemotherapy had a median OS of 8.6 months [5] - The trial demonstrated increased progression-free survival (PFS) and duration of response (DoR) in the VCN-01 treatment group, with median PFS of 7.0 months compared to 4.6 months for the control group [5] Safety Profile - VCN-01 was well-tolerated, with adverse events being transient and reversible, consistent with prior clinical trials [3][4] - The most common adverse events included pyrexia, flu-like illness, and elevated transaminases, which were less frequent after the second dose of VCN-01 [3] Future Directions - The positive data from the VIRAGE trial is expected to facilitate engagement with industry partners and support the design of a Phase 3 confirmatory trial [3][4]

NEW HOPE, Pa., April 29, 2025 (GLOBE NEWSWIRE) -- Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO, "Orchestra BioMed" or the "Company"), a biomedical company accelerating high-impact technologies to patients through risk-reward sharing partnerships, today announced that the U.S. Food and Drug Administration ("FDA") has approved its Investigational Device Exemption ("IDE") amendment to initiate an updated design of the Company's planned Virtue SAB in the Treatment of Coronary ISR Trial ("Virtue Trial"). The ID ...

Cardiff Oncology (CRDF) Q4 2024 Earnings Call February 27, 2025 04:30 PM ET Company Participants Kiki Patel - PrincipalMark Erlander - CEOJames Levine - Chief Financial OfficerAlexander Kelly - Biotech Equity Research Associate Conference Call Participants Joseph Catanzaro - Director & Senior Equity AnalystAndy Hsieh - Research AnalystRobert Burns - MD & Senior Healthcare AnalystAlbert Lowe - Senior Research Analyst Operator Welcome to the Cardiff Oncology Fourth Quarter twenty twenty four Financial Results ...