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Food & Drug Administration (FDA)

Brainstorm’s NurOwn stem cell treatment for ALS readies for phase III

December 19, 2016 By Sarah Faulkner

BrainStorm Cell Therapeutics

Brainstorm Cell Therapeutics (NSDQ:BCLI) said today that it’s preparing for a phase III trial of its NurOwn stem cell treatment, after meeting with the FDA about a biologic license application. The company is developing adult stem cell therapies derived from autologous bone marrow cells to treat neurodegenerative diseases, such as ALS. Hackensack, N.J.-based Brainstorm is planning […]

Filed Under: Clinical Trials, Featured, Food & Drug Administration (FDA), Neurological, Stem Cells Tagged With: Brainstorm Cell Therapeutics

Galderma wins FDA nod for dermal fillers

December 15, 2016 By Sarah Faulkner

Galderma wins FDA nod for dermal fillers

Galderma said today that it won FDA approval for 2 of its products to treat nasolabial folds, or “laugh lines”.  The Fort Worth, Texas-based company’s Restylane Refyne and Restylane Defyne are made with XpresHAn technology to manufacture injectable gels with customized hyaluronic acid crosslinking in each product. The federal watchdog’s approval was based on 2 […]

Filed Under: Clinical Trials, Featured, Food & Drug Administration (FDA), Regulatory/Compliance, Surgical Tagged With: Galderma

FDA approves first bioresorbable scaffold with autologous cells for cartilage repair

December 14, 2016 By Sarah Faulkner

vericel

Vericel Corp (NSDQ:VCEL) shares soared 56% today after the Cambridge, Mass.-based company said the FDA approved its bioresorbable scaffold for cartilage repair. The product, Maci, is the 1st FDA-approved implant to use healthy cartilage tissue from a patient’s own knee to grow cells on the scaffold. “Different cartilage defects require different treatments, so therapy must be […]

Filed Under: Featured, Food & Drug Administration (FDA), Orthopedics, Regulatory/Compliance, Stem Cells, Surgical, Wall Street Beat Tagged With: Vericel Corp

AcelRx seeks FDA nod for non-invasive sufentanil painkiller

December 13, 2016 By Sarah Faulkner

AcelRx Pharmaceuticals

AcelRx Pharmaceuticals (NSDQ:ACRX) said today that it submitted a new drug application to the FDA for its ARX-04 sublingual sufentanil tablet. The non-invasive compound has been studied as a treatment for patients experiencing moderate or severe acute pain and is administered in a medically supervised setting using a disposable, pre-filled, single-dose applicator. The Redwood City, Calif.-based […]

Filed Under: Featured, Food & Drug Administration (FDA), Pain Management, Pharmaceuticals, Regulatory/Compliance Tagged With: AcelRx

Flexion seeks FDA nod for osteoarthritis steroid injection

December 12, 2016 By Sarah Faulkner

Flexion Therapeutics (NSDQ:FLXN) said today that it submitted a new drug application to the FDA for its extended-release steroid injection Zilretta. The Burlington, Mass.-based company won Fast Track status from the watchdog for its osteoarthritis injection last year. The new drug application is based on data from a pivotal phase III clinical trial evaluating Zilretta in […]

Filed Under: Featured, Food & Drug Administration (FDA), Orthopedics, Pain Management, Regulatory/Compliance Tagged With: Flexion Therapeutics

SRI wins $150m grant to develop HIV prevention products

December 7, 2016 By Sarah Faulkner

SRI wins $150m grant to develop HIV prevention products

SRI International said today that it landed a $150 million contract from the National Institutes of Health‘s National Institute of Allergy and Infectious Diseases and the Division of AIDS to support the development of HIV microbicides and other pre-exposure agents. According to the 7-year deal, the research institute will provide preclinical product development services for non-vaccine […]

Filed Under: Clinical Trials, Discovery, Featured, Food & Drug Administration (FDA), Funding Roundup, Preclinical Trials, Research & Development Tagged With: National Institutes of Health, SRI International

Scilex touts data for novel lidocaine patch

December 5, 2016 By Sarah Faulkner

Scilex Pharmaceuticals

Sorrento Therapeutics (NSDQ:SRNE) subsidiary Scilex Pharmaceuticals said today that its lidocaine patch, ZTlido, met primary and secondary endpoints in a pivotal study comparing the patch to Endo Pharmaceutical‘s Lidoderm patch. The data will be used to resubmit a new drug application to the FDA in mid-2017, the Malvern, Pa.-based company said. The clinical trial evaluated Scilex’s […]

Filed Under: Clinical Trials, Featured, Food & Drug Administration (FDA), Pain Management, Pharmaceuticals, Wall Street Beat Tagged With: Endo Pharmaceuticals, Scilex Pharmaceuticals, Sorrento Therapeutics

J&J’s Evarrest fibrin sealant patch wins expanded indication for hemostasis

December 2, 2016 By Sarah Faulkner

Ethicon

Johnson & Johnson (NYSE:JNJ) subsidiary Ethicon said today that the FDA approved an expanded indication for its Evarrest fibrin sealant patch as an supplementary hemostat. With the expanded indication, the patch can be used with manual compression as an adjunct to hemostasis in adult surgery patients, when standard surgical techniques to control bleeding such as suture […]

Filed Under: Drug-Device Combinations, Featured, Food & Drug Administration (FDA), Regulatory/Compliance, Surgical Tagged With: Ethicon, johnsonandjohnson

Pharma execs assess landscape under President Trump

December 2, 2016 By Sarah Faulkner

capitol hill

Executives from U.S. drugmakers such as Regeneron Pharmaceuticals and Pfizer talked about the possible changes awaiting the industry under President-elect Donald Trump at the Forbes Healthcare Summit this week. After he was elected, pharmaceutical stocks surged as investors concluded the threat of action on drug pricing had lessened. Trump has said he wants to repeal […]

Filed Under: Featured, Food & Drug Administration (FDA), Legal News, Pharmaceuticals, Policy, Wall Street Beat Tagged With: Allergan, Merck, Pfizer Inc., Regeneron

Nordisk touts Tresiba insulin injection data

November 30, 2016 By Sarah Faulkner

Novo Nordisk

Novo Nordisk (NYSE:NVO) said today that data from the Devote clinical trial indicated that its injected insulin, Tresiba, reduced the risk of severe hypoglycemia when compared to insulin glargine. The trial enrolled more than 7,500 type 2 diabetes patients at high risk of adverse cardiovascular events and treated them for 2 years with either Tresiba or insulin glargine […]

Filed Under: Clinical Trials, Diabetes, Featured, Food & Drug Administration (FDA), Pharmaceuticals Tagged With: Novo Nordisk

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