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Latest Articles

Ultragenyx Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $210 Million

Ultragenyx Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $210 Million

Ultragenyx Pharmaceutical announced a definitive agreement to sell its Rare Pediatric Disease Priority Review Voucher (PRV) for $210 million. The PRV was granted following FDA approval of Genelycos™, a treatment for glycogen storage disease type Ia. The sale is expected to provide non-dilutive capital to advance Ultragenyx's pipeline and support pr…

Propanc Biopharma Reports Data Showing 90% Tumor Growth Inhibition with PRP in Pancreatic Cancer Models, Contrasting Profile with Revolution Medicines’ Daraxonrasib

Propanc Biopharma Reports Data Showing 90% Tumor Growth Inhibition with PRP in Pancreatic Cancer Models, Contrasting Profile with Revolution Medicines’ Daraxonrasib

Propanc Biopharma announced promising preclinical data for its lead candidate PRP, demonstrating over 90% tumor growth inhibition, reduced metastases, and tumor microenvironment remodeling in pancreatic ductal adenocarcinoma models. PRP offers a distinct mechanism from Revolution Medicines' FDA-approved daraxonrasib, targeting cancer pathways not a…

TOMI Environmental Solutions Confirms Readiness to Support Biosecurity Preparedness and Front-Line Response Worldwide

TOMI Environmental Solutions Confirms Readiness to Support Biosecurity Preparedness and Front-Line Response Worldwide

TOMI Environmental Solutions, trading on NASDAQ under TOMZ, confirmed its preparedness to support global biosecurity efforts through its disinfection technology and services. The company highlighted its capability to assist hospitals, laboratories, and government agencies in response to potential outbreaks, using its SteraMist systems. This announc…

RenovoRx Advances TAMP™ into Borderline Resectable Pancreatic Cancer with First Patient Enrolled in Investigator-Initiated PRISM-TAMP Trial

RenovoRx Advances TAMP™ into Borderline Resectable Pancreatic Cancer with First Patient Enrolled in Investigator-Initiated PRISM-TAMP Trial

RenovoRx has enrolled the first patient in the PRISM-TAMP investigator-initiated trial, evaluating neoadjuvant intra-arterial gemcitabine delivery via their TAMP platform for borderline resectable pancreatic ductal adenocarcinoma. This marks a clinical expansion beyond their ongoing Phase III for locally advanced pancreatic cancer, with results ant…

Progyny, Inc. Selling Season Pacing to Record Level, Revealing Critical Insights on Latest Market Dynamics

Progyny, Inc. Selling Season Pacing to Record Level, Revealing Critical Insights on Latest Market Dynamics

Progyny, Inc., a leader in women's health and family-building solutions, announced that its current annual selling season is pacing to a record level with an expected addition of 1.2 million new covered lives in the first half of 2027. The company's fertility solutions address rising medical cost inflation by offering employers programs that improv…

SciSparc: Subsidiary NeuroThera Labs’ CliniQuantum Reports Successful Quantum-Enabled Analysis of Billions of Gene Combinations Using Real-World Clinical Data on an S&P 500 Company’s Quantum Architecture

SciSparc: Subsidiary NeuroThera Labs’ CliniQuantum Reports Successful Quantum-Enabled Analysis of Billions of Gene Combinations Using Real-World Clinical Data on an S&P 500 Company’s Quantum Architecture

SciSparc Ltd., through its majority-owned subsidiary NeuroThera Labs and further its subsidiary CliniQuantum, announced a successful demonstration of a quantum-enabled GPU-accelerated platform that analyzed over 7 billion potential three-gene combinations in real-world clinical data. Utilizing a single NVIDIA T4 GPU, their platform achieved approxi…

FDA Grants SeaStar Medical Breakthrough Device Designation for its SCD Therapy for the Treatment of Hyperinflammation in Adult Patients with Sepsis or a Septic Condition

FDA Grants SeaStar Medical Breakthrough Device Designation for its SCD Therapy for the Treatment of Hyperinflammation in Adult Patients with Sepsis or a Septic Condition

SeaStar Medical received FDA Breakthrough Device Designation for its Selective Cytopheretic Device (SCD) therapy to treat hyperinflammation in adult patients with sepsis or septic conditions. This designation accelerates development and review processes, marking the seventh breakthrough designation for the SCD platform across multiple indications. …

FuelCell Energy Announces Chief Financial Officer Transition

FuelCell Energy Announces Chief Financial Officer Transition

FuelCell Energy, Inc. announced a planned transition in its CFO position with Michael Bishop stepping down after 15 years and Matthew Latino succeeding him. The company reaffirmed its target to achieve positive Adjusted EBITDA in Q4 fiscal 2027, contingent on production increases and backlog conversion. FuelCell Energy is focused on scaling manufac…

MAIA Biotechnology Achieves Patient Enrollment Milestones in Ongoing Phase 2 and Pivotal Phase 3 Clinical Trials in Non-Small Cell Lung Cancer

MAIA Biotechnology Achieves Patient Enrollment Milestones in Ongoing Phase 2 and Pivotal Phase 3 Clinical Trials in Non-Small Cell Lung Cancer

MAIA Biotechnology announced completion of patient enrollment in Part C of its Phase 2 THIO-101 trial and achieving 65% enrollment in its pivotal Phase 3 THIO-104 trial investigating ateganosine combined with checkpoint inhibitors for treatment of advanced non-small cell lung cancer (NSCLC). Interim Phase 2 data show high disease control rates sign…

EXL schedules third quarter 2026 financial results conference call

EXL schedules third quarter 2026 financial results conference call

ExlService Holdings, Inc., a global data and AI company, will release its financial results for the third quarter ended September 30, 2026, on October 27, after market close. The company will host a conference call on October 28 featuring executives discussing operational and financial outcomes. EXL serves multiple industries including insurance, h…

Safe Pro Expects Record 2,300% Revenue Growth in Q3 2026 Driven by Multiple Government Contracts for AI-Powered Threat Detection and Mapping

Safe Pro Expects Record 2,300% Revenue Growth in Q3 2026 Driven by Multiple Government Contracts for AI-Powered Threat Detection and Mapping

Safe Pro Group Inc., a U.S.-based AI-enabled defense and security solutions company, announced preliminary expectations of a 2,300% year-over-year revenue growth in Q3 2026, driven by multiple U.S. Army and Air Force subcontracts. The company's innovative AI threat detection and battlefield mapping technology is gaining traction with government age…

Esperion Reaches Settlement Agreement with Sixth ANDA Filer Not to Market Generic Version of NEXLETOL® (bempedoic acid) & NEXLIZET® (bempedoic acid & ezetimibe) Prior to April 19, 2040

Esperion Reaches Settlement Agreement with Sixth ANDA Filer Not to Market Generic Version of NEXLETOL® (bempedoic acid) & NEXLIZET® (bempedoic acid & ezetimibe) Prior to April 19, 2040

Esperion Therapeutics has reached a settlement agreement with Renata Limited preventing the marketing of generic versions of its cholesterol-lowering drugs NEXLETOL and NEXLIZET in the US until April 19, 2040, reinforcing its patent protection. Ongoing litigations with other generic filers continue. Esperion, wholly owned by ARCHIMED, focuses on ca…