Le Lézard
Classified in: Health, Science and technology
Subject: FDA

Curcugen® Curcumin Formulation Attains GRAS status


LANDING, N.J., March 16, 2021 /PRNewswire/ -- CURCUGEN®, DolCas Biotech's bioavailability-enhanced, water-dispersible curcuminoid complex, has received Self-Affirmed Generally Recognized As Safe (GRAS) status. This designation was unanimously accorded by an independent panel of scientific experts and based on scientific procedures, concluding that CURCUGEN meets FDA's definition of safety when used as an ingredient in yogurt, nutrition bars, smoothies, and other food and beverage products at levels of 40-60 mg per serving.

The panel concurrently determined an Acceptable Daily Intake (ADI) of CURCUGEN® at 210 mg/person/day, using both JECFA standards and which falls in line with the 2010 EFSA scientific opinion on the "conservative estimate" for assessing exposure to curcumin. The committee also determined an upper limit up to 1400 mg/person/day in the same food formats which it considered was safe and meet the requirements of GRAS, as defined by the FDA. This conclusion was drawn directly from a battery of toxicological studies performed using CURCUGEN.

Next-gen qualities

DolCas' new curcumin formula is a 100% natural, water-dispersible curcumin ingredient. It is a proprietary 98.5% turmeric-based preparation of turmeric oleoresin extract and fresh turmeric rhizome extract derived from Curcuma longa L. The company applies a SELF Dtm platform technology to optimize the oleoresin base so that its benefits can be fully realized. At the same time it eliminates the need to complement the curcuminoids with other, non-turmeric ingredients, or reconstitute it with displaced turmeric ingredients.

The independent GRAS conclusion included an appraisal of the manufacturing process, product specifications, as well as consideration of opinions by other regulatory bodies around the globe that verified its Current Good Manufacturing Practice (CGMP) status.

"In contrast to certain generic curcumin products currently on the market, our formulation preserves the original complex of curcuminoids, essential oils, and polar resins within the optimized oleoresin matrix," explains Dr. Shavon Jackson-Michel, Director of Medical & Scientific Affairs for DolCas Biotech. "This supports its superior bioactive and holistic qualities? CURCUGEN is time-tested and its efficacy has been scientifically explored for its positive role in gut health and mood, as well as mitigating inflammation."

CURCUGEN's 98.5% turmeric formulation provides a high concentration of curcuminoids at a 50% standard, without omitting other, well-characterized and functional turmeric actives, including turmeric essential oils and polysaccharides. This synergism is what elicits the clinical benefits associated with the brand at doses as low as 500 mg/day, and is pivotal in the brand's novel dispersion mechanism.

"CURCUGEN's fidelity to the turmeric rhizome, its low effective dose, and diverse delivery potential combined with therapeutic application and the new high-limit independent safety affirmation opens the brand to be among the most trusted in the industry," extols Jackson-Michel.

DolCas will take the brand to the highest level of safety appraisal with the FDA in a comprehensive GRAS submission within the next few months. "With the new Self-GRAS status in place, we can continue studying the brand and broaden its integration into beverages, food and confectionary, and expand its application to additional categories, including sports nutrition and general wellbeing," concludes Mr. KG Rao, CEO & President of DolCas Biotech.

About Dolcas Biotech, LLC

Dolcas Biotech, LLC. was established in 2007 as an extension to its generic ingredients corporation, Orcas Naturals.  The company centers its operations on the creation, introduction, marketing and distribution of unique botanical and nutritional products to the world and supports these endeavors with ongoing research and regulatory processes to ensure maximum efficacy and to position its branded portfolio of ingredients for success.

In 2017, Dolcas Biotech established its own manufacturing arm, DolCas Botanosys in Bikaner, India helping to vertically integrate the company and its sister corporations in the procurement of high-quality ingredients. The company has been designated one of '50 Most Innovative Companies to Watch' in 2020 by The Silicon Review. 

 

 

Company Contact:

 

 

Press Contact:

DolCas Biotech, LLC

NutriPR

Dr. Shavon Jackson-Michel

Liat Simha

Director of Medical & Scientific Affairs

Tel: +972-9-9742893

Tel: 973-347-1958 ext. 217

E-mail: [email protected]

Email: [email protected]

Website: www.nutripr.com

Web: www.dolcas-biotech.com

Twitter: @LiatSimha

 

SOURCE DolCas Biotech


These press releases may also interest you

at 18:30
BrainStorm Cell Therapeutics Inc. , a leading developer of adult stem cell therapeutics for neurodegenerative diseases, today announced the promotion of Dr. Bob Dagher to Executive Vice President and Chief Medical Officer. In addition, after four...

at 18:16
Globe Life Inc. will release First Quarter 2024 earnings after the market closes on Monday, April 22, 2024.  At that time, a copy of the Company's First Quarter 2024 earnings press release and any other financial and statistical information about...

at 17:56
The Canadian Cancer Society commends the increases in taxes on tobacco and e-cigarettes in today's federal budget.  The budget increases tobacco taxes by $4.00 per carton of 200 cigarettes effective at midnight, and increases e-cigarette taxes by 12%...

at 17:45
Alvotech and Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. , today announced that the U.S. Food and Drug Administration (FDA) has approved SELARSDI (ustekinumab-aekn) injection for subcutaneous use, as a biosimilar to...

at 17:31
The rise in demand for dental lasers is mainly driven by the growing occurrence of dental issues like bleeding or inflamed gums, tooth decay, and root infections. Furthermore, advancements in dental technology play a significant role in fostering...

at 17:26
Amgen today provided an update regarding the results of the Phase 2a COURSE trial for TEZSPIRE® (tezepelumab-ekko) in chronic obstructive pulmonary disease (COPD), which were accepted for presentation in the Clinical Trials Symposium at The American...



News published on and distributed by: