Latest News on Clinical Trials
China National Medical Products Administration Approves Sinovant’s Clinical Trial Application for Derazantinib
- Chinese registrational clinical trial for derazantinib to begin in 2H 2019 Sinovant Sciences today announced that its Clinical Trial Application (CTA) for derazantinib has been accepted by the Center for Drug Evaluation at the China National Medical Products...
Axovant Announces Dosing of First Patient in Second Cohort of SUNRISE-PD Phase 2 Trial of AXO-Lenti-PD
-Up to 6 patients to be enrolled in the second cohort, initial data expected in fourth quarter 2019- -Oral presentation at the Annual Meeting of the American Society of Gene and Cell Therapy- BASEL, Switzerland, April 30, 2019 (GLOBE NEWSWIRE) -- Axovant Gene...
Dynacure Announces Approval of Clinical Trial Application for DYN101, an Antisense Medicine to Treat Rare Disease ‘Centronuclear Myopathies’
Company expects to initiate Phase 1 / 2 study 'Unite-CNM' in 2H2019 Dynacure, a clinical stage drug development company focused on improving the lives of patients with rare and orphan disorders, today announced that The Medicines and Healthcare products Regulatory...
Belite Bio Announces FDA Approval of Investigational New Drug (IND) for Phase 1 Clinical Trial of LBS-008 to Treat Macular Degeneration and Stargardt Disease
Belite Bio, a drug development company targeting currently untreatable conditions in ophthalmology and metabolic diseases, announced today that the U.S. Food and Drug Administration (FDA) has approved its Investigational New Drug application (IND) for LBS-008...
PPD Recognized for Exceptional Quality of Collaboration with Clinical Research Sites
Pharmaceutical Product Development, LLC (PPD), a leading global contract research organization (CRO), was named the winner of the CRO Quality Award from the Association of Clinical Research Professionals (ACRP) and The Avoca Groupduring the recent ACRP annual...
ReNeuron Announces Presentation of Updated Efficacy and Safety Data from Retinitis Pigmentosa Study at the Sixth Annual Retinal Cell and Gene Therapy Innovation Summit
hRPC Cell Therapy Demonstrates Sustained and Further Improvement in Vision at 60 and 120 Days in First Cohort of Phase 2a study in Retinitis Pigmentosa Mean Change from Baseline in Visual Acuity of +23 Letters to Date LONDON, April 26, 2019 /PRNewswire/ -- ReNeuron...
WINTHER trial results: Comprehensive tumor profiling promises new therapeutic options for patients with advanced cancer
The WINTHER trial***, NCT01856296, led by investigators from Vall d'Hebron Institute of Oncology - VHIO (Spain), Chaim Sheba Medical Center (Israel) (Raanan Berger), Gustave Roussy (France) (Jean-Charles Soria), Centre Léon Bérard (France) (Pierre Saintigny), Segal...
Cavion to Present Results of Phase 2 Essential Tremor Clinical Trial in Platform Presentation at the American Academy of Neurology
Presentation to provide overview of Phase 2 T-CALM study design, results and clinical path forward Cavion, Inc., a leading clinical stage biotechnology company committed to developing novel therapeutics for people with neurological diseases, announced today that the...
Rexgenero Presents Update on Phase III Clinical Trials with REX-001, a Cell-based Therapy for Critical Limb Ischaemia
At the Alliance for Regenerative Medicine’s Cell and Gene Therapy ‘Meeting on the Med’ in Barcelona Rexgenero, a regenerative medicine company pioneering the development of advanced cell-based therapies to treat critical limb ischaemia (CLI), today presented an update...
Results from Clinical Trial Show Progenics’ PyL (18F-DCFPyL) PSMA PET/CT Imaging Agent Changes Management Plans for More Than 87% of Patients
Data from a Prospectively Designed Independent Trial of 130 Patients showed that PyL upstaged and downstaged disease in 65.5% of patients Progenics Pharmaceuticals, Inc. (PGNX), an oncology company developing innovative targeted medicines and artificial intelligence...
WVU Cancer Institute participating in immunotherapy clinical trial
The WVU Cancer Institute is recruiting participants for an immunotherapy clinical trial for patients with metastatic melanoma or recurrent or metastatic head and neck squamous cell carcinoma. The trial will evaluate the effectiveness of the immunotherapy drug SD-101...
Provention Bio Completes Enrollment of Phase 2a PRINCE Clinical Trial with PRV-6527 in Patients with Moderate to Severe Crohn’s Disease
Provention Bio, Inc. (Nasdaq: PRVB), a clinical stage biopharmaceutical company dedicated to intercepting and preventing immune-mediated diseases, today announced that it has completed the enrollment in its Phase 2a PRINCE (PRovention Investigation in Crohn's DiseasE)...
Blood Samples Help Match Cancer Patients to Early Phase Clinical Trials
Scientists could help match cancer patients with no other treatment options to clinical trials with experimental medicines, by analysing the genetic faults in a sample of their blood, according to research published in Nature Medicine*. The researchers, funded by...
Data Management in the Face of Growing Trial Complexity
Leveraging innovative processes and technology to help tackle the industry’s toughest data challenges According to Tufts Center for the Study of Drug Development, the average time to build and release a clinical study database is more than 73 days and the average time...
Molecular Profiling of Cancer Patients Uncovers Combination Treatments in I-PREDICT Study
Clinical trials in oncology may benefit from relying on personalized combination therapies rather than matching patients to monotherapies, according to a new analysis from the Investigation of Profile-Related Evidence Determining Individualized Cancer Therapy...
Vineti and Marker Therapeutics announce strategic partnership to support diverse cell therapy portfolio
Vineti Inc., the leading software platform of record for personalized therapeutics, today announced a new partnership to advance and scale Marker Therapeutics’ T cell therapy pipeline. Marker Therapeutics is a clinical-stage immuno-oncology company specializing in the...
U.S. Food and Drug Administration Accepts Biologics License Application for Eptinezumab
Alder BioPharmaceuticals, Inc. (NASDAQ: ALDR), a biopharmaceutical company focused on developing novel therapeutic antibodies for the treatment of migraine, today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the Biologics License...
AEGEA Medical Completes Enrollment in PACE MX, the Third Study Assessing Long-Term Access to the Uterine Cavity after Endometrial Ablation with Water Vapor
AEGEA Medical announced today that it has completed enrollment in the Post-Ablation Cavity Evaluation Mexico (PACE MX) clinical study of women who previously underwent endometrial ablation as part of a pivotal trial of AEGEA’s Mara™ Water Vapor Ablation Treatment. The...
Patients living with Spinal Muscular Atrophy (SMA) in the province of Saskatchewan gain access to SPINRAZA™ (nusinersen)
The Government of the province of Saskatchewan has informed treating physicians that it will grant access to SPINRAZA™ to patients living with Spinal Muscular Atrophy (SMA) Saskatchewan is the second province after the province of Quebec to grant broad access...
European Investment Bank (EIB) Extends Financing Agreement to €24 Million Total in Support of BiondVax’s Universal Flu Vaccine Ongoing Pivotal Phase 3 Clinical Trial
€4 million extension to 2017 financing agreement BiondVax Pharmaceuticals Ltd. (Nasdaq: BVXV), announced today that the Management Committee of the European Investment Bank (EIB) agreed to extend the 2017 financing agreement with BiondVax by an additional €4 million....
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