CEL-SCI Corporation recently had a productive meeting with the U.S. Food and Drug Administration (FDA) regarding the approval of Multikine for head and neck cancer treatment. The FDA recognizes the urgent need for better therapies in this field and is willing to collaborate with CEL-SCI to demonstrate the effectiveness of Multikine as a potential treatment option. Additionally, CEL-SCI is active..
Quest Diagnostics has recently launched a groundbreaking prostate cancer test that aims to improve the diagnosis and grading of this disease.   This innovative lab service utilizes Envision Science's exclusive biomarkers and technology, with the ultimate goal of enhancing the accuracy of prostate cancer diagnosis and grading. The launch of this new test was announced by Quest Diagnostics, th..
F-star Therapeutics, an invoX company, has announced a strategic collaboration and license agreement with Takeda to discover and develop next-generation multi-specific antibodies. The collaboration will focus on using F-star's proprietary platforms to research and develop immunotherapies for cancer patients. Under the agreement, F-star and Takeda will work together to research and develop novel ..
Immutep (Formerly known as Prima Biomed) Limited has successfully completed an A$80 million capital raise to support its clinical development pipeline. The company, a clinical-stage biotechnology firm specializing in LAG-3 immunotherapies for cancer and autoimmune diseases, believes that the new funding will fully support its current and expanded clinical program until Q1 CY2026. With a pro-form..
Jubilant Therapeutics is preparing to begin Phase II and first-in-human trials later in 2023 with two Orphan Drug Designations, an advantageous safety profile, and enhanced therapeutic indices. The company's pipeline uses their Therapeutic Index and Brain Exposure Optimization (TIBEO) discovery engine to identify candidate molecules with improved therapeutic indices and the ability to penetrate ..
Jubilant Therapeutics, a precision oncology and immunology-focused biotech, is set to begin Phase II and first-in-human trials in 2023 with two Orphan Drug Designations. Their pipeline is generated entirely in-house using their unique discovery engine called the Therapeutic Index and Brain Exposure Optimization (TIBEO) which identifies candidate molecules with enhanced therapeutic indices that c..
Jubilant Therapeutics is gearing up for Phase II and first-in-human trials in 2023 with its pipeline of precision medicines that offer safety and therapeutic advantages in cancer and immunology. The company's drug discovery approach focuses on developing candidates through clinical proof of concept, partnering those assets with companies to advance them through late-stage clinical development an..
Jubilant Therapeutics is preparing for Phase II and first-in-human trials later in 2023, with two Orphan Drug Designations, an advantageous safety profile and enhanced therapeutic indices. The company's pipeline is generated 100% in-house using its Therapeutic Index and Brain Exposure Optimization (TIBEO) discovery engine, which permits the identification of candidate molecules with enhanced the..
