drug
LETROZOLE
Marketedupdated 3mo agoby Yiling Pharmaceutical Ltd
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 2indications
investigational
Breast Cancer
all catalysts(9)
approval · 9
Jun 3, 2011
approval
LETROZOLE — FDA approval
LETROZOLE
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May 15, 2012
approval
LETROZOLE — FDA approval
LETROZOLE
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Jul 19, 2014
approval
LETROZOLE — FDA approval
LETROZOLE
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Feb 13, 2015
approval
LETROZOLE — FDA approval
LETROZOLE
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Feb 13, 2015
approval
LETROZOLE — FDA approval
LETROZOLE
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Apr 2, 2021
approval
LETROZOLE — FDA approval
LETROZOLE
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Apr 2, 2021
approval
LETROZOLE — FDA approval
LETROZOLE
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Oct 1, 2025
approval
LETROZOLE — FDA approval
LETROZOLE
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Oct 1, 2025
approval
LETROZOLE — FDA approval
LETROZOLE
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Trials studying LETROZOLE
- phase3An Adjuvant Endocrine-based Therapy Study of Camizestrant (AZD9833) in ER+/HER2- Early Breast Cancer (CAMBRIA-2)
- phase3Elacestrant for Treating ER+/HER2- Breast Cancer Patients With ctDNA Relapse (TREAT ctDNA)
- phase2ORION-1: Study of AVZO-023 as a Single Agent and in Combination With AVZO-021, and/or Endocrine Therapy in Advanced Solid Tumors
- phase3BGB-43395 Plus Letrozole Versus CDK4/6i Plus Letrozole for Patients With Advanced or Metastatic HR+/HER2- Breast Cancer Who Have Not Received Prior Treatment for Advanced or Metastatic Disease
- phase3A Study Evaluating the Efficacy and Safety of Inavolisib Plus CDK4/6 Inhibitor and Letrozole vs Placebo + CDK4/6i and Letrozole in Participants With Endocrine-Sensitive PIK3CA-Mutated, Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer
- phase2A Phase II, Single-Arm Study of RAD001 (Everolimus), Letrozole, and Metformin in Patients With Advanced or Recurrent Endometrial Carcinoma
- phase2Study of GVV858 as a Single Agent or in Combination With Endocrine Therapy in Patients With HR+/HER2- Breast Cancer and Other Advanced Solid Tumors
- phase3Saruparib (AZD5305) Plus Camizestrant or Plus Endocrine Therapy, Compared With CDK4/6 Inhibitor Plus Endocrine Therapy or Plus Camizestrant in HR-Positive, HER2-Negative (IHC 0, 1+, 2+/ ISH Non-amplified), BRCA1, BRCA2, or PALB2m Advanced Breast Cancer
Patent cliff
source: FDA Orange Bookfirst barrier falls
Sep 17, 2027
~1.1 years out
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (11)
- Apr 14, 2036formulationUS 10799506
- Apr 14, 2036formulationUS 12064434
- Apr 14, 2036formulationUS 12419894
- Aug 7, 2034method-of-use (U-3998)US 12544380
- Nov 9, 2031compositionUS 9193732
- Nov 9, 2031method-of-use (U-3264)US 9868739
- Mar 13, 2031compositionUS 84153554.6y
- May 25, 2030compositionUS 86859803.8y
- Dec 9, 2029method-of-use (U-3264)US 89626303.3y
- Aug 20, 2029method-of-use (U-3264)US 94161363.0y
- Jun 17, 2028compositionUS 83242251.8y
FDA exclusivities (1)
- Sep 17, 2027I-951Indication (3y)1.1y
News(3)
- Opinion: Telehealth abortion with mifepristone continues, with backup plans still in placeRestricting telehealth prescribing of mifepristone wouldn't spell the end of telehealth medication abortion, writes OB-GYN Christine Henneberg.stat · 2mo ago
- Poll Results Highlight Breast Cancer Abstracts of Interest at ASCO 2026Readers share their opinions on some of the most talked-about breast cancer abstracts they’re looking forward to seeing at ASCO 2026.onclive · 3mo ago
- ASCO 2026 HR+ and HER2+ Breast Cancer Preview: Read up on the Insights to Know Before You GoBreast cancer experts spotlight the abstracts they’re most excited to see at the 2026 ASCO Annual Meeting.onclive · 3mo ago
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