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Therapeutic Area

SGLT2 Inhibitor

Therapeutic area intelligence for SGLT2 Inhibitor with 22 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
22
Catalysts
0
Companies
8

Companies

AstraZeneca →
Aurobindo Pharma →
Centaur Pharmaceuticals →
Jiangsu Hansoh Pharma →
Merck →
Sciegen Pharmaceuticals →
Sun Pharma →
Teva →

Assets

Apotex →
BRENZAVVY →
Canagliflozin →
Dapagliflozin →
Empagliflozin →
Farxiga →
Inventia →
Janssen →
QTERN →
STEGLATRO →
STEGLUJAN →
TRAVERE →

Recent signals(22)

RegulatoryAugust 4, 2026

FDA Accepts Dapagliflozin Application from Centaur Pharmaceuticals

The FDA has accepted the application ANDA220679 for dapagliflozin from Centaur Pharmaceuticals.

StrategyAugust 2, 2026

FDA Submission Overview for Dapagliflozin by Sciegen Pharmaceuticals

Sciegen Pharmaceuticals has submitted an original application for dapagliflozin under ANDA219408, currently in TA status.

StrategyJuly 29, 2026

FDA Submission Update for Canagliflozin by Teva Pharmaceuticals

Teva Pharmaceuticals has submitted an application for Canagliflozin under ANDA210451, currently under standard review.

StrategyJuly 28, 2026

FDA Approves Canagliflozin Application by Aurobindo Pharma

The FDA has approved the ANDA210386 application for Canagliflozin submitted by Aurobindo Pharma.

CompetitiveJuly 26, 2026

FDA Accepts Application for Canagliflozin by Apotex

The FDA has accepted the application ANDA210449 for Canagliflozin submitted by Apotex.

StrategyJuly 24, 2026

Teva's ANDA Submission for Canagliflozin Receives TA Status

Teva Pharmaceuticals has submitted an ANDA for Canagliflozin, currently under standard review with TA status.

RegulatoryJuly 23, 2026

FDA Approves Supplemental Application for QTERN (Dapagliflozin/Saxagliptin)

The FDA has approved a supplemental application for QTERN, a combination of dapagliflozin and saxagliptin.

RegulatoryJuly 23, 2026

FDA Accepts Supplement for STEGLUJAN (Ertugliflozin/Sitagliptin)

The FDA has accepted a supplemental application for STEGLUJAN, a combination of ertugliflozin and sitagliptin.

RegulatoryJuly 23, 2026

FDA Accepts Supplement for STEGLATRO (Ertugliflozin) by Merck

The FDA has accepted a supplemental application for STEGLATRO (ertugliflozin) from Merck.

RegulatoryJuly 23, 2026

FDA Approves Supplemental Application for Farxiga (Dapagliflozin)

The FDA has approved a supplemental application for Farxiga, an SGLT2 inhibitor developed by AstraZeneca.

RegulatoryJuly 22, 2026

FDA Accepts Supplemental NDA for BRENZAVVY (Bexagliflozin)

The FDA has accepted a supplemental NDA for BRENZAVVY, indicating progress in its regulatory review.

RegulatoryJuly 22, 2026

FDA Accepts Supplement for INVOKANA (Canagliflozin) by Janssen

The FDA has accepted a supplemental application for INVOKANA (canagliflozin) from Janssen Pharmaceuticals.

RegulatoryJuly 21, 2026

FDA Accepts Supplement Application for Dapagliflozin by Inventia

The FDA has accepted the supplemental application for dapagliflozin submitted by Inventia.

RegulatoryJuly 20, 2026

FDA Accepts Supplemental Application for Dapagliflozin and Metformin Hydrochloride

The FDA has accepted a supplemental application for dapagliflozin and metformin hydrochloride submitted by Sun Pharma.

CompetitiveJuly 20, 2026

Aurobindo Pharma submits ANDA for Empagliflozin

Aurobindo Pharma has submitted an Abbreviated New Drug Application (ANDA) for Empagliflozin.

CompetitiveJuly 13, 2026

Centaur Pharmaceuticals submits ANDA for Dapagliflozin

Centaur Pharmaceuticals has submitted an Abbreviated New Drug Application (ANDA) for Dapagliflozin.

CompetitiveJuly 11, 2026

FDA Submission for Dapagliflozin by Sciegen Pharmaceuticals

Sciegen Pharmaceuticals has submitted an original ANDA for Dapagliflozin, currently under standard review.

RegulatoryJuly 5, 2026

Aurobindo Pharma's ANDA for Canagliflozin Receives Approval Status

Aurobindo Pharma's ANDA210386 for Canagliflozin has received an approval status (AP) from the FDA.

StrategyJuly 3, 2026

FDA Accepts Application for Canagliflozin by Apotex

The FDA has accepted the application for Canagliflozin submitted by Apotex under ANDA210449.

RegulatoryJune 22, 2026

FDA Accepts Supplement Application for Dapagliflozin by Inventia

The FDA has accepted the supplemental application for dapagliflozin submitted by Inventia.

RegulatoryJune 10, 2026

FDA Accepts Supplement for FILSPARI (SPARSENTAN) by TRAVERE

The FDA has accepted a supplemental application for FILSPARI (SPARSENTAN) from TRAVERE.

CompetitiveJune 6, 2026

FDA Submission for Dapagliflozin by Jiangsu Hansoh Pharma

Jiangsu Hansoh Pharma has submitted an original application (ANDA216119) for Dapagliflozin, currently under standard review.

Upcoming catalysts

No catalysts indexed for this entity yet.

Indications

Diabetes →

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