Combining the corticosteroid methylprednisolone and Jakafi (ruxolitinib), an approved oral therapy for bone marrow disorders, is showing promising effectiveness in heavily pre-treated multiple myeloma patients in an ongoing Phase 1 trial. Findings to date from this open-label study (NCT03110822), which is being sponsored by Onco Therapeutics, showed that the combination not only elicited promising responses but was…
Author: Chris
Bavencio Approved in EU as First-line Maintenance Therapy for Bladder Cancer
The European Commission (EC) has approved Bavencio (avelumab) as a first-line maintenance treatment for adults with advanced urothelial carcinoma, the most common form of bladder cancer, whose disease did not progress after platinum-based chemotherapy. This decision follows a positive recommendation from the Committee for Medicinal Products for Human Use, a branch of the European Medicines Agency. Bavencio…
Nonprofit Highlights Importance of Global Teamwork for World Cancer Day
In honor of World Cancer Day on Feb. 4, the Breast International Group (BIG) emphasized the importance of wide-scale cooperation in efforts to advance cancer research. “None of BIG’s achievements would be possible without the willingness to work together,” stated a press release highlighting some of the clinical trials that are supported by BIG, an…
Combining Imaging Methods May Reduce Need for Tumor Biopsies
Combining two imaging methods can provide a more accurate sampling of single tumors — like those found in ovarian cancer — thus allowing doctors to capture the diverse cancer cells in the tumor with fewer biopsies, a new study found. The study, “Ultrasound-guided targeted biopsies of CT-based radiomic tumour habitats: technical development and initial experience…
Patients, Caregivers Urged to Get COVID-19 Vaccines ASAP
People with Alzheimer’s disease, as well as their caregivers, are being urged — on social media and via press releases — to get COVID-19 vaccines as soon as possible. That’s the recommendation of the Medical, Scientific and Memory Screening Advisory Board of the Alzheimer’s Foundation of America (AFA). “Getting vaccinated is one of the most…
EPI-7386 Combo Therapies Enter Trial for Certain mCRPC Patients
Essa Pharma has entered a clinical collaboration with Janssen to evaluate its small molecule inhibitor EPI-7386, in combination with either Erleada (apalutamide) or Zytiga (abiraterone acetate) plus prednisone, for patients with metastatic castration-resistant prostate cancer (mCRPC). Under the terms of the agreement, Janssen will conduct up to two Phase 1/2 clinical trials evaluating these combinations in…
$10M Gift to Open Myeloma Research Center at Ohio State
A new research center at Ohio State University (OSU) aims to speed work into the discovery and development of more effective treatments for those with multiple myeloma. The Riney Family Foundation Myeloma Center for Advanced Research Excellence (Myeloma CARE) is being established through a $10 million gift from the Paula and Rodger Riney Foundation to the…
Retifanlimab Under FDA Priority Review for Advanced Anal Canal Cancer
Retifanlimab is under review in the U.S. as a treatment for advanced squamous cell carcinoma of the anal canal (SCAC), a rare cancer of the digestive system, in adults who are unable to receive, or whose disease progressed after, initial platinum-based chemotherapy. Incyte’s biologics licence application (BLA) to the U.S. Food and Drug Administration (FDA)…
Enhertu Approved in EU for Inoperable, Advanced Breast Cancer
The European Commission has conditionally approved Enhertu (trastuzumab deruxtecan) for adults in the EU with inoperable or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 based regimens. A conditional approval is granted when the benefits of a medication regulators say still requires additional data or testing are found to outweigh its potential…
Non-invasive Neurostimulation Device Wins FDA’s Breakthrough Status
Cognito Therapeutic’s neurostimulation device — a next-generation digital therapeutic designed to treat memory and cognition symptoms in Alzheimer’s disease — has been granted a breakthrough device designation by the U.S. Food and Drug Administration (FDA). The device, part of a new class of disease-modifying digital therapies, uses proprietary, non-invasive neurostimulation technology developed by Massachusetts Institute…