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…
Conditions
Conditions
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…
NantKwest Launches Phase 1 Trial to Assess Investigational Cell Therapy for Solid Cancers
This post was originally published on this site A first-in-human Phase 1 clinical trial has been launched to assess the effects of NantKwest’s investigational PD-L1 t-haNK cell therapy in patients with locally advanced or metastatic solid cancers. The authorization to start the trial came after the U.S. Food and Drug Administration (FDA) completed a review…
$169K Raised by Local California Chapter in Annual Campaign of the Leukemia & Lymphoma Society
This post was originally published on this site Nearly $169,000 was raised to support the Leukemia & Lymphoma Society’s research, legislative advocacy, and patient support efforts by one of its chapter’s Man & Woman of the Year campaign. California residents Nancy Whitman and John Romley won the title for the Silicon Valley & Monterey Bay…
Carriers of CHRFAM7A gene Less Responsive to Cholinesterase Inhibitors, Study Suggests
This post was originally published on this site Alzheimer’s disease patients carrying a gene found only in humans, called CHRFAM7A, are less responsive to cholinesterase inhibitors, a new study reports. These findings may explain why some therapeutic benefits seen in animal studies have failed to translate to patients. Kinga Szigeti, MD, PhD, director of the…
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
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…
BRCA Testing for Ovarian Cancer Patients Could Be Decided by Family History and Age, Study Suggests
This post was originally published on this site Women with ovarian cancer who have a family history of breast or ovarian cancer, and are younger than 45 if breast cancer in a near relative makes up that history, are more likely to have inherited BRCA mutations and could benefit from a genetic test to see if they…
ADT Linked to Higher Alzheimer’s and Dementia Risk in Older Prostate Cancer Patients, Study Suggests
This post was originally published on this site Men with prostate cancer who undergo treatment with androgen deprivation therapy (ADT) — a form of hormone therapy that aims to slow disease progression by reducing the levels of male hormones — may be more likely to develop Alzheimer’s disease and dementia, a large database study reports.…
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
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
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…











