Sentences with phrase «received food and drug»

«Agents that block the proteins — CDK4 / 6 inhibitors — have received Food and Drug administration approval for some patients with metastatic breast cancer, but they've also shown promise against others types of tumors in clinical trials.

Only one such treatment has so far received Food and Drug Administration approval (a therapy to treat bladder cancer), though others are in the pipeline.

Sidel has received Food and Drug Administration (FDA) approval for its Aseptic Combi Predis ™ FMa blow fill seal filler following tests run at a dairy customer in North America.

The DEA has already received the Food and Drug Administration's recommendation on the rescheduling, which is a key part of the rescheduling process stipulated by the Controlled Substance Act, says Russell Baer, a special agent at the DEA's office of public affairs.

The biotech received Food and Drug Administration (FDA) approval for its drug to treat the rare blood cancer acute myeloid lymphoma (AML), which will be marketed as Idhifa, on Tuesday.

Not exact matches

The company has received approval from the Food and Drug Administration to test for carrier status of 36 genetically - transmitted conditions.

Fremanezumab had been expected to receive the nod from the U.S. Food and Drug Administration in June, which would have likely made it the second to the crucial American market after Aimovig, which is expected to be approved next month.

SAN JOSE, Calif., April 25, 2018 (GLOBE NEWSWIRE)-- Align Technology, Inc. (NASDAQ: ALGN) today announced that the company has received approval from the China Food and Drug Administration (CFDA) to market the iTero Element intraoral scanner in China.

The only way to get around the ban is to receive approval from the U.S. Food and Drug Administration (FDA).

Nearly a year after it clashed with the Food and Drug Administration over labeling on its dried fruit and nut bars, KIND has received approval to use the word «healthy» as part of its marketing.

Datum Biotech, DePuy Synthes product introduction and updates... Episurf Medical enters distribution agreement with Pacific Medical Systems in Hong Kong... Advanced Biomedcal Technologies receives approval from the CHina Food and Drug Administration... Fidia Farmaceutici, McGinley Orthopedics announces milestone of surgeries using IntelliSense HandHeld Robotic Drill

DuPont Protection Technologies received notification from the Center for Devices and Radiological Health (CDRH) at the U.S. Food and Drug Administration affirming the functional equivalence of transition Tyvek ® to current Tyvek ® for sterile medical packaging.

A month prior, Hampton Creek received confirmation of «GRAS» (generally recognized as safe) status for its mung bean protein isolate from the US Food and Drug Administration.

There is speculation the Wattle deal involves an Australian distribution agreement, and not a potential milestone in receiving an important regulatory approval from the China Food and Drug Administration ahead of new regulations starting on January 1 for all infant formula companies selling into China.

Based on the emails I continue to receive, there seems to be confusion on the part of many regarding the ingredients contained in this product as well as the Food and Drug Administration's (FDA) position on malt extract in labeled gluten - free foods.

Recently, Sidel received approval from the US Food and Drug Administration (FDA) for its Aseptic Combi Predis ™ FMa blow fill seal filler.

Food and Drug Administration (FDA)-- The FDA receives a total of almost $ 2.6 billion in discretionary funding in the bill, an increase of $ 23 million over the fiscal year 2014 enacted level.

Physicians who encounter adverse effects in infants who have been receiving drug - contaminated human milk are urged to document these effects in a communication to the Food and Drug Administration (http://www.fda.gov/medwatch/index.html) and to the Committee on Drdrug - contaminated human milk are urged to document these effects in a communication to the Food and Drug Administration (http://www.fda.gov/medwatch/index.html) and to the Committee on DrDrug Administration (http://www.fda.gov/medwatch/index.html) and to the Committee on Drugs.

This year, GE received approval from the U.S. Food and Drug Administration to make the SIGNA ™ Premier available for sale.

However, co-authors Richard Lockey, MD, and Chen Hsing Lin, MD suggest pregnant women receive the same benefit following the Food and Drug Administration and Environmental Protection Agency's recommendation to consume 8 - 12 ounces (2 - 3 servings) of low mercury fish a week.

The drug, trade named Mylotarg, received accelerated approval from the U.S. Food and Drug Administration in 2000 for treatment of AML in adudrug, trade named Mylotarg, received accelerated approval from the U.S. Food and Drug Administration in 2000 for treatment of AML in aduDrug Administration in 2000 for treatment of AML in adults.

PreScience Labs, a U.S. company founded by Geschwind, received approval for a phase I study from the U.S. Food and Drug Administration in 2013.

* Update: On April 6 Medtronic announced that its Micra Transcatheter Pacing System had become the first leadless pacemaker to receive U.S. Food and Drug Administration approval.

The only «noninvasive» glucose meter to have received U.S. Food and Drug Administration (FDA) approval is no longer on the market.

The U.S. Food and Drug Administration approved the drug on Nov. 20 for patients with myeloma who have received at least one previous therDrug Administration approved the drug on Nov. 20 for patients with myeloma who have received at least one previous therdrug on Nov. 20 for patients with myeloma who have received at least one previous therapy.

Although the trial first received the go - ahead in January last year, it was put on hold the following August by the US Food and Drug Administration, which demanded further evidence that the treatment wouldn't cause cysts like those seen in some animal studies.

In 2014 GW Pharmaceuticals, a British drug company, received special permission from the U.S. Food and Drug Administration to test its pharmaceutical version of cannabidiol, called Epidiodrug company, received special permission from the U.S. Food and Drug Administration to test its pharmaceutical version of cannabidiol, called EpidioDrug Administration to test its pharmaceutical version of cannabidiol, called Epidiolex.

Because of the legislation, a FDA spokesperson noted in an email, «the agency will not receive or review INDs [Investigational New Drug applications] for human subject research utilizing genetic modification of embryos for the prevention of transmission of mitochondrial disease in FY 2016 and human subject research using these technologies can not be conducted in compliance with the Federal Food, Drug, and Cosmetic Act and FDA's implementing regulations.»

The cancer cells» defense strategy can be overcome by immune checkpoint inhibitor agents, including anti-PD-1 / PD - L1 antibodies, several kinds of which have received fast - track approval from the U.S. Food and Drug Administration (FDA).

On August 18, the day arrived: Flibanserin — a failed antidepressant — received approval from the Food and Drug Administration to boost sexual desire in women.

«The Food and Drug Administration (FDA) has announced the approval of Inflectra (infliximab - dyyb), the first biosimilar to receive approval in the U.S. for the treatment of rheumatic diseases, including rheumatoid arthritis and psoriatic arthritis.

In 2008, SPOC received US Food and Drug Administration 510 clearance, after Phase 1 clinical trials at NYU Medical Center and a pilot study at Kaiser Permanente Hospital.

All three have received fast track status from the United States Food and Drug Administration.»

A first - of - its - kind gene therapy received approval from the Food and Drug Administration on Tuesday to treat a rare, inherited form of childhood blindness.

Imbio, a startup launched from the University of Michigan in 2007, has just received clearance from the U.S. Food and Drug Administration to sell its software platform based on U-M research.

The issues that received the lowest deference scores were biotech foods, legalizing drug use, animal testing, evolution, mandatory health insurance, and gay adoption.

Whaley said the company responds to requests that come through the U.S. Food and Drug Administration and has no say in who ultimately had received the product.

Fifty days after the mice were born, one group was injected three times a week with Hsp70 and another received Riluzole, the only drug approved by the Food and Drug Administration to combat drug approved by the Food and Drug Administration to combat Drug Administration to combat ALS.

In April 2015, it received a U.S. Food and Drug Administration (FDA) Breakthrough Therapy designation.

Da Vinci, which costs about $ 2 million and received U.S. Food and Drug Administration approval in 2000, allows surgeons to manipulate laparoscopic instruments and an endoscopic camera attached to four robotic arms.

Geron Corporation of Menlo Park, California, received the green light from the US Food and Drug Administration this week to use cells derived from hESCs to treat people with acute spinal cord injuries.

Vanderbilt University scientists have received notification from the U.S. Food and Drug Administration (FDA) that testing in humans may proceed for an investigational new drug after more than 10 years of research by scientists at Vanderbilt University and Vanderbilt University Medical CenDrug Administration (FDA) that testing in humans may proceed for an investigational new drug after more than 10 years of research by scientists at Vanderbilt University and Vanderbilt University Medical Cendrug after more than 10 years of research by scientists at Vanderbilt University and Vanderbilt University Medical Center.

For example, Novartis and the University of Pennsylvania's lead candidate (CTL019) for treating a range of hematological malignancies received breakthrough status from the US Food and Drug Administration (FDA) in 2014, permitting access to an expedited drug development pathway for high unmet medical needs Drug Administration (FDA) in 2014, permitting access to an expedited drug development pathway for high unmet medical needs drug development pathway for high unmet medical needs (1).

Snowdon has received approximately $ 4 million in grants and contracts from the National Institutes of Health, the U.S. Food & Drug Administration, the New Jersey Commission on Science & Technology, the Department of Defense and the private sector.

Cagan's lab recently received approval from the US Food and Drug Administration to begin a clinical trial in colorectal and medullary thyroid carcinoma to see if fly avatars can successfully help guide patient care.

Mycophenolate mofetil is approved by the U.S. Food and Drug Administration (FDA) to prevent organ rejection in people who have received a kidney, heart, or liver transplant.

Many of these products are reaching late - phase trials with the potential to receive final approval and marketing authorization from regulatory agencies such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA).

NEW YORK, NY — April 30, 2010 — The Cancer Research Institute celebrates yesterday's announcement of the first therapeutic cancer vaccine to receive approval from the U.S. Food and Drug Administration.

Last year, SAV001 - H received approval by the United States Food and Drug Administration (FDA) to start human clinical trials.

For example, Novartis and the University of Pennsylvania's lead candidate (CTL019) for treating a range of hematological malignancies received breakthrough status from the US Food and Drug Administration (FDA) in 2014, permitting access to an expedited drug development pathway for high unmet medical neDrug Administration (FDA) in 2014, permitting access to an expedited drug development pathway for high unmet medical nedrug development pathway for high unmet medical needs.