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Asset / Drug

AZURITY

Drug and asset intelligence for AZURITY with 14 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
11
Catalysts
3
Stage
Development stage unavailable

Sponsor company

Bristol Myers Squibb →

Mechanism of action

Combination Therapy

Recent signals(11)

RegulatoryAugust 12, 2026

FDA accepts supplemental NDA for WIDAPLIK by AZURITY

The FDA has accepted the supplemental NDA for WIDAPLIK (NDA219423) submitted by AZURITY, with a standard review priority.

RegulatoryAugust 11, 2026

FDA Accepts Supplement for XATMEP (NDA 208400) by Azurity

The FDA has accepted a supplemental application for XATMEP (NDA 208400), a methotrexate sodium product from Azurity, under standard review priority.

Regulatory
August 11, 2026

FDA Accepts Supplement for FERAHEME by AZURITY

The FDA has accepted a supplemental application for FERAHEME (ferumoxytol) submitted by AZURITY, with a standard review priority.

RegulatoryAugust 2, 2026

FDA Acceptance of Supplement Application for MYHIBBIN by AZURITY

The FDA has accepted a supplemental application for MYHIBBIN (NDA216482) from AZURITY.

RegulatoryJuly 26, 2026

FDA Accepts Supplement Application for Danziten (Nilotinib Tartrate)

The FDA has accepted a supplemental application for Danziten, an oncology drug containing nilotinib tartrate.

RegulatoryJuly 21, 2026

FDA Accepts Supplemental NDA for WIDAPLIK by Azurity

The FDA has accepted a supplemental NDA for WIDAPLIK, which includes amlodipine besylate, indapamide, and telmisartan.

RegulatoryJuly 21, 2026

FDA Accepts Supplement for FERAHEME by AZURITY

The FDA has accepted a supplemental application for FERAHEME, an iron replacement therapy.

RegulatoryJuly 21, 2026

FDA Accepts Supplemental Application for XATMEP (Methotrexate Sodium)

The FDA has accepted a supplemental application for XATMEP, a formulation of methotrexate sodium.

RegulatoryJuly 8, 2026

FDA Submission Status Update for ABANTA (Apixaban) by AZURITY

The FDA has received a submission for ABANTA (Apixaban) under NDA221024 from AZURITY, currently under standard review.

RegulatoryJuly 3, 2026

FDA Accepts Supplement Application for Danziten (Nilotinib Tartrate)

The FDA has accepted a supplemental application for Danziten, which contains nilotinib tartrate.

RegulatoryJune 23, 2026

FDA Review Status Update for Aprepitant NDA218754 by Azurity

The FDA has received a new drug application (NDA218754) for Aprepitant from Azurity, currently under standard review.

Upcoming milestones

No catalysts indexed for this entity yet.

Related catalysts(3)

Topline Data

Bristol Myers Squibb — AZURITY

July 8, 2026 · N/A

Topline Data

— AZURITY

July 3, 2026 · N/A

Topline Data

— Azurity

June 23, 2026 · N/A

Indications

No related entities indexed yet.

Therapeutic areas

Anticoagulant →
Cardiovascular →
Cardiovascular · Anticoagulant →
Chemotherapy →
Combination Therapy →
Hematology →
Immunology →
Iron Replacement →
Oncology →
Oncology · Tyrosine Kinase Inhibitor →
Renal Transplantation →
Tyrosine Kinase Inhibitor →

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