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FDA approves Johnson & Johnson’s nasal spray for depression

FDA approves standalone use of J&J’s ketamine-derived depression treatment

The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression, the company said on Tuesday.

Fox Business · 7h

J&J's ketamine-derived nasal spray approved by FDA to treat depression

Johnson & Johnson's ketamine-derived nasal spray has been approved as a standalone treatment to fight depression for those who had an inadequate response to oral antidepressants.

KSAT · 4h

FDA approves first nasal spray for major depression disorder

The U.S. Food and Drug Administration on Tuesday approved the first nasal spray that will help with treating major depressive disorder.

WFAE · 6h

FDA allows standalone use of nasal spray antidepressant Spravato (esketamine)

The FDA says esketamine, an antidepressant derived from the anesthetic and party drug ketamine, can now be prescribed on its own. It was approved in 2019 to treat severe depression.

WAVY Norfolk on MSN · 7h

Nose spray to treat depression? FDA approves first-of-its-kind medicine

The U.S. Food and Drug Administration has approved a nose spray to help treat depression, Johnson & Johnson announced Tuesday.

FDA, Atara Biotherapeutics

AOL · 6h

FDA Places Clinical Hold On Atara Biotherapeutics' Two Cell Therapy Programs

On Tuesday, the U.S. Food and Drug Administration (FDA) placed a clinical hold on Atara Biotherapeutics, Inc.’s (NASDAQ:ATRA) active Investigational New Drug (IND) applications. These INDs include the EBVALLO (tabelecleucel) program for patients two years of age and older with Epstein-Barr virus-positive post-transplant lymphoproliferative disease (EBV+ PTLD),

Business Insider · 7h

Atara Biotherapeutics Faces Uncertainty Amid FDA Clinical Hold and Financing Needs, Resulting in Hold Rating

Atara Biotherapeutics (ATRA – Research Report), the Healthcare sector company, was revisited by a Wall Street analyst today. Analyst Benjamin

MarketWatch · 16h

Atara's New Drug Applications Placed on Hold by FDA

Atara Biotherapeutics said the U.S. Food and Drug Administration placed a clinical hold on its active investigational new drug applications. The biotechnology company said the FDA put a hold on its Ebvallo and ATA3219 programs due to compliance issues at a third-party manufacturing facility.

11hon MSN

FDA proposes mandatory front-of-package nutrition labels to combat spike in chronic diseases

The U.S. Food and Drug Administration (FDA) is demanding increased, in-your-face food transparency when it comes to nutrition ...

STAT19h

Three former FDA officials: Here’s what Trump and his nominees need to know

The FDA is the leading science-based consumer protection agency in the world. Three former senior officials write about what ...

13hon MSN

More than a dozen cats dead or sickened by bird flu in raw pet food, FDA says

More than a dozen cats have been killed or sickened by bird flu that is spreading in raw food products, the Food and Drug ...

14h

FDA makes key decision on Zyn nicotine pouches

In a statement, the FDA said it has authorized the marketing and sale of Philip Morris International’s Zyn nicotine pouches.

STAT13h

A next-generation form of chemotherapy wins FDA approval

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1don MSN

RFK Jr. wants to improve Americans’ health. Here’s some advice from the outgoing FDA chief

Robert F. Kennedy Jr. has big plans for the FDA if he's confirmed as Secretary of Health and Human Services. FDA Commissioner ...

Healio12h

FDA approves Datroway for advanced breast cancer

The FDA approved datopotamab deruxtecan-dlnk for treatment of certain patients with advanced breast cancer.The indication ...

The National Law Review12h

FDA Issues New Recommendations on Use of AI for Medical Devices, Drugs, and Biologics

In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued ...

15hon MSNOpinion

Food companies want to confuse consumers. The FDA must push back.

Food companies criticize the science supporting front-of-package labeling, delay public consultation periods, push for their ...

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FDA approves Johnson & Johnson’s nasal spray for depression

FDA, Atara Biotherapeutics

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