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Samus Therapeutics Launches Phase 1 Trial of Tau-targeting Therapy

Samus Therapeutics Launches Phase 1 Trial of Tau-targeting Therapy

This post was originally published on this site Following the approval of its investigational new drug (IND) application by the U.S. Food and Drug Administration (FDA), Samus Therapeutics is launching a Phase 1 trial in the United States to evaluate the safety of its investigational therapy PU-AD, an epichaperome inhibitor, for the treatment of Alzheimer’s…

FDA Approves Clinical Testing of Minerva’s CAR T-cell Therapy for Metastatic BC

FDA Approves Clinical Testing of Minerva’s CAR T-cell Therapy for Metastatic BC

This post was originally published on this site Minerva Biotechnologies will soon start the first human trials testing its investigational therapy huMNC2-CAR44, a CAR T-cell immunotherapy intended for breast cancer that has spread to other parts of the body. The announcement comes after the U.S. Food and Drug Administration (FDA) approved the company’s investigational new…

Anixa Partners with Cleveland Clinic to Take Breast Cancer Vaccine to Human Trials

Anixa Partners with Cleveland Clinic to Take Breast Cancer Vaccine to Human Trials

This post was originally published on this site Anixa Biosciences, a leading company developing anti-cancer immunotherapies, is partnering with the Cleveland Clinic to advance a vaccine against triple-negative breast cancer (TNBC) to testing in humans. “We are pleased to be able to work with Anixa to advance this technology into human trials,” Cleveland Clinic researcher…

CHMP Favors Empliciti Triple Combo to Treat Advanced Multiple Myeloma Patients in EU

CHMP Favors Empliciti Triple Combo to Treat Advanced Multiple Myeloma Patients in EU

This post was originally published on this site The Committee for Medicinal Products for Human Use (CHMP), a branch of the European Medicines Agency (EMA), has recommended that Empliciti (elotuzumab) in combination with Pomalyst (pomalidomide) and low-dose dexamethasone be approved to treat adults with relapsed or refractory multiple myeloma in Europe. The therapy, collectively known as the…

ONCOS-102, Keytruda Combo May Reduce Tumor Size in Treatment-resistant Melanoma, Early Trial Data Show

ONCOS-102, Keytruda Combo May Reduce Tumor Size in Treatment-resistant Melanoma, Early Trial Data Show

This post was originally published on this site Melanoma patients who become resistant to immune checkpoint inhibitors may regain susceptibility to such treatments after receiving Targovax‘s immune activator ONCOS-102, early clinical trial findings suggest. The trial is testing a combination of ONCOS-102 and the immune checkpoint inhibitor Keytruda (pembrolizumab) in advanced or surgery-ineligible melanoma patients…

FDA Approves Rituxan Biosimilar Ruxience for Non-Hodgkin’s Lymphoma

FDA Approves Rituxan Biosimilar Ruxience for Non-Hodgkin’s Lymphoma

This post was originally published on this site The U.S. Food and Drug Administration (FDA) has approved Pfizer’s Ruxience (rituximab-pvvr), a biosimilar to Rituxan (rituximab), for all non-Hodgkin’s lymphoma indications of its reference product, the company announced. The therapy was also approved for people with chronic lymphocytic leukemia (CLL), as well as granulomatosis with polyangiitis (GPA)…

Rare Case of Spinal Sarcoidosis Provides Guidelines for Diagnosis, Management

Rare Case of Spinal Sarcoidosis Provides Guidelines for Diagnosis, Management

This post was originally published on this site A new report describes a woman with a very rare case of sarcoidosis involving only the spine who entered full remission after surgical removal of the lesion followed by treatment with corticosteroids. Based on this case report, researchers advised that cases of spinal sarcoidosis should be managed…