Moleculin Biotech (MBRX) has received FDA feedback and guidance on its IND amendment that has allowed a reduction in the size of its Phase 3 ...

Moleculin Biotech (MBRX) has received first country regulatory approval in Europe to begin recruiting for its Phase 3 pivotal trial protocol ...

Once you agree, your application is submitted to Goldman Sachs for approval. After your approval, you can request to have your physical titanium Apple Card delivered, with Apple saying it should ...

(CNN) – The U.S. Food and Drug Administration approved the first new type of pain medication in more than two decades, and it’s not an opioid. The drug is suzetrigine under the brand name ...

Registered book titles with the "Human Authored" logo are entered into a public database. The seal of approval is by no means a rejection of new technology, emphasizes the organization's ...

Aston Martin Lagonda Global Holdings Plc designs, creates, and exports cars. Its sports cars are manufactured in Gaydon with its luxury DBX SUV range manufactured in St. Athan, Wales. The company ...

The Food and Drug Administration (FDA) has approved Grafapex ™ (treosulfan ... aged 1 year and older with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Findings showed OS ...

It’s officially 2025 and with the new year, the weather is getting chillier, the days are feeling a little grey and, so naturally, we’re spending all our time inside looking to update our ...

Dana-Farber Cancer Institute researchers have identified factors that determine whether donor lymphocyte infusion (DLI), a standard therapy for patients with acute myeloid leukemia (AML ...

The approval was based on data from the phase 3 MC-FludT.14/L trial (NCT00822393), which enrolled 570 patients aged 18-70 years who had AML or MDS. The patients were randomly assigned to receive ...

Acute myeloid leukaemia (AML) is mainly characterized by an increase in the number of myeloid cells in the bone marrow and a decrease in mature cells, accounting for 28% of leukaemia cases ...