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  1. pharmadog
  2. ›drugs
  3. ›Myfembree
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(estradiol + norethindrone acetate + relugolix)

Marketedupdated 3mo ago
by Sumitomo Pharma America Inc
Approved
community read0 votes

all catalysts(0)

nothing on the calendar yet

Trials studying (estradiol + norethindrone acetate + relugolix)

  • phase4Surgical Myomectomy Followed by Oral Myfembree Versus Standard of Care Trial (SOUL)withdrawn

Patent cliff

source: FDA Orange Book
first barrier falls
Jan 28, 2029
~2.5 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (8)

  • Nov 5, 2042formulationUS 12551447
  • May 3, 2038method-of-use (U-2360)US 11793812
  • Sep 29, 2037method-of-use (U-3129)US 11033551
  • Sep 29, 2037method-of-use (U-3129)US 11957684
  • Sep 27, 2033compositionUS 11795178
  • Sep 27, 2033compositionUS 12325714
  • Jan 28, 2029compositionUS 73009352.5y
  • Jan 28, 2026compositionUS 8058280

FDA exclusivities (1)

  • Jan 27, 2026M-289Method (3y)

News(0)

no news has mentioned this drug yet

brand
Myfembree
generic
(estradiol + norethindrone acetate + relugolix)
indication
Pain
phase
marketed
Data sources
ClinicalTrials.gov
last refreshed 2h ago
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