AstraZeneca gets CDSCO nod for Dapagliflozin in CKD

Published On 2021-01-17 10:00 GMT   |   Update On 2021-01-17 11:26 GMT
Advertisement

New Delhi: The Subject Expert Committee (SEC), operative under the Central Drugs Standard Control Organization (CDSCO), has given its nod to AstraZeneca's proposal of Dapagliflozin for an additional indication. The CDSCO panel has approved the drug for the treatment of Chronic Kidney Disease patients up to Stage III (eGFR of greater than or equal to 30ml/min/1.73m2).

AstraZeneca has made available the drug in India in brand names of Forxiga 

Advertisement

Dapagliflozin 5mg and 10mg was approved in India on 25th Feb 2015 for Type 2 Diabetes Mellitus patients to improve glycemic control. Thereafter, the company received approval on 30th July 2019 to include additional information about the therapeutic effects of Dapagliflozin on glycemic control and cardiovascular event under clinical section. On 3rd July 2020, Astrazeneca further received approval for the additional indication – HEART FAILURE with reduced ejection fraction for Dapagliflozin 10mg tablets, making it the first and only drug approved in India for the management of Heart Failure with reduced Ejection fraction. In addition, Astrazeneca also presented and published positive results from DAPA-CKD study and submitted the data to the regulatory agency for new indication review and approval. 

The proposal for using Dapagliflozin film coated Tablet 10mg for additional indication had been presented by AstraZeneca before the SEC committee of CDSCO. The firm further requested the CDSCO panel for the local clinical trial waiver as well.

Read also: NPPA Brings Remoglifozin, Metformin Combination Under Price Control, Pulls Up Mankind, Intas Pharma For Unapproved Launch

The SEC committee of CDSCO, in its  83rd meeting, held on 07.01.2021 & 08.01.2021 at CDSCO HQ New Delhi discussed all the Cardiovascular and Renal proposals submitted by pharmaceutical companies and made some recommendations regarding the same.

After detailed deliberation the committee recommended for grant of permission for the treatment of patients of Chronic Kidney Disease (CKD) up to Stage III (eGFR of greater than or equal to 30ml/min/1.73m2).


Tags:    

Disclaimer: This website is primarily for healthcare professionals. The content here does not replace medical advice and should not be used as medical, diagnostic, endorsement, treatment, or prescription advice. Medical science evolves rapidly, and we strive to keep our information current. If you find any discrepancies, please contact us at corrections@medicaldialogues.in. Read our Correction Policy here. Nothing here should be used as a substitute for medical advice, diagnosis, or treatment. We do not endorse any healthcare advice that contradicts a physician's guidance. Use of this site is subject to our Terms of Use, Privacy Policy, and Advertisement Policy. For more details, read our Full Disclaimer here.

NOTE: Join us in combating medical misinformation. If you encounter a questionable health, medical, or medical education claim, email us at factcheck@medicaldialogues.in for evaluation.

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News