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  1. pharmadog
  2. ›drugs
  3. ›Latisse
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Lumigan

Marketedupdated 5mo ago
by $ABBV AbbVie Inc.
Approved
community read0 votes

🐶 often sniffed alongside

top 5
  • drugBIMATOPROST3 co-mentions · 3 sources
  • drugbimatoprost CR3 co-mentions · 3 sources
  • drugbimatoprost SR3 co-mentions · 3 sources
  • tagApproval2 co-mentions · 1 sources
  • tagRecall2 co-mentions · 2 sources

Small molecule drug with a maximum clinical stage of Approval (across all indications), with 6 approved and 8 investigational indications.

all catalysts(1)

approval · 1
Sep 22, 2025
approval
$AMRX19.77-0.18%
1y ago
BIMATOPROST — FDA approval
Lumigan
→

Trials studying Lumigan

  • phase3A Study to Evaluate Efficacy and Safety of YSBP Compared to Lumigan in Patients With Glaucoma or Ocular Hypertensionrecruitingn=600
  • phase2A Study to Evaluate the Efficacy and Safety of OTX-TIC (Travoprost) Intracameral Implant for Patients With Open-angle Glaucoma (OAG) or Ocular Hypertension (OHT)completedn=83
  • phase3Long-term Safety and Efficacy Extension Trial of Bimatoprost SRcompletedn=455
  • phase2AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertensionrecruitingn=96
  • phase4Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensive Medication Userecruitingn=20
  • phase3Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compared to Timolol Ophthalmic Solution (Rhine)recruitingn=400
  • phase3Evaluation of the Safety and Efficacy of the Bimatoprost Implant System Used in Combination With the SpyGlass IOL Compared to Timolol Ophthalmic Solution (Rhone)recruitingn=400
  • N/AEvaluation of the Safety and Effectiveness of the Bimatoprost Implant System / IOL Combination in Patients With Ocular Hypertension or Mild to Moderate Open-angle Glaucomacompletedn=24

Patent cliff

source: FDA Orange Book
first barrier falls
Dec 19, 2026
84 days

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

patents (9)

  • Jun 8, 2036formulationUS 10314780
  • Oct 31, 2034formulationUS 9492316
  • Oct 31, 2034method-of-use (U-2759)US 9980974
  • Jul 15, 2031compositionUS 86291854.8y
  • Apr 24, 2029formulationUS 77993362.6y
  • Jun 13, 2027compositionUS 7851504260d
  • Apr 7, 2027method-of-use (U-2759)US 8206737193d
  • Dec 19, 2026formulationUS 1044154384d
  • Dec 19, 2026formulationUS 914942884d

FDA exclusivities (1)

  • Sep 9, 2028NDFNew Dosage Form (3y)2.0y

News(0)

no news has mentioned this drug yet

brand
Latisse
generic
bimatoprost
MOA
Prostanoid FP receptor agonist
indication
Ocular Hypertension
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 2h ago
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