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Bimatoprost

Generic Name
Bimatoprost
Brand Names
Durysta, Latisse, Lumigan
Drug Type
Small Molecule
Chemical Formula
C25H37NO4
CAS Number
155206-00-1
Unique Ingredient Identifier
QXS94885MZ
Background

Bimatoprost, also known as Latisse or Lumigan, belongs to a group of drugs called prostamides, which are synthetic structural analogs of prostaglandin. Bimatoprost, marketed by Allergan, is administered in both the ophthalmic solution and implant form. It has the ability to reduce ocular hypotension, proving effective in conditions such as ocular hypertension and glaucoma. Bimatoprost is also used to treat eyelash hypotrichosis, or sparse eyelash growth. It was initially approved by the FDA in 2001 for ocular hypertension and later approved for hypothrichosis in 2008, as eyelash growth became a desirable adverse effect for patients using this drug.

Indication

Bimatoprost is used for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

These patients must be intolerant to other intraocular pressure lowering medications or inadequately responsive to other treatments.

Bimatoprost is also indicated to treat eyelash hypotrichosis.

Associated Conditions
Hypotrichosis of the eyelashes, Increased Intra Ocular Pressure (IOP)

Observational Study of Lumigan® 0.01% Treatment for Patients With Primary Open Angle Glaucoma or Ocular Hypertension

Completed
Conditions
Glaucoma, Open-Angle
Ocular Hypertension
Interventions
First Posted Date
2011-12-12
Last Posted Date
2014-03-28
Lead Sponsor
Allergan
Target Recruit Count
387
Registration Number
NCT01489670

Assessment of Intraocular Pressure (IOP) Control in Subjects With Open-Angle Glaucoma or Ocular Hypertension Treated With Travoprost 0.004% (TRAVATAN® Z) or Bimatoprost 0.01% (LUMIGAN®)

Phase 4
Completed
Conditions
Glaucoma
Ocular Hypertension
Open-Angle Glaucoma
Interventions
First Posted Date
2011-11-03
Last Posted Date
2013-09-13
Lead Sponsor
Alcon Research
Target Recruit Count
84
Registration Number
NCT01464424

Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Prominence

Phase 4
Completed
Conditions
Hypotrichosis
Interventions
First Posted Date
2011-10-07
Last Posted Date
2013-05-22
Lead Sponsor
Allergan
Target Recruit Count
88
Registration Number
NCT01448525

A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma

First Posted Date
2011-08-31
Last Posted Date
2015-10-02
Lead Sponsor
Allergan
Target Recruit Count
6
Registration Number
NCT01426113

Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypotrichosis

Phase 3
Completed
Conditions
Eyelash Hypotrichosis
Interventions
First Posted Date
2011-07-12
Last Posted Date
2019-07-08
Lead Sponsor
Allergan
Target Recruit Count
173
Registration Number
NCT01391273

Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy-Induced Eyelash Hypotrichosis

Phase 3
Completed
Conditions
Eyelash Hypotrichosis
Interventions
First Posted Date
2011-07-12
Last Posted Date
2019-07-08
Lead Sponsor
Allergan
Target Recruit Count
36
Registration Number
NCT01391286

Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: Latisse Versus Placebo

Phase 4
Completed
Conditions
Hypotrichosis
Interventions
First Posted Date
2011-07-06
Last Posted Date
2012-06-15
Lead Sponsor
Kenneth Beer
Target Recruit Count
20
Registration Number
NCT01387906
Locations
🇺🇸

Kenneth R. Beer, M.D. ,PA, West Palm Beach, Florida, United States

Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female Pattern Hair Loss

First Posted Date
2011-03-29
Last Posted Date
2014-04-09
Lead Sponsor
Allergan
Target Recruit Count
306
Registration Number
NCT01325350

Safety and Efficacy Study of Bimatoprost in the Treatment of Men With Androgenic Alopecia

First Posted Date
2011-03-29
Last Posted Date
2014-04-10
Lead Sponsor
Allergan
Target Recruit Count
307
Registration Number
NCT01325337

Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension

Phase 4
Completed
Conditions
Glaucoma
Ocular Hypertension
Interventions
First Posted Date
2011-02-18
Last Posted Date
2018-09-17
Lead Sponsor
Allergan
Target Recruit Count
806
Registration Number
NCT01298700
Locations
🇮🇱

Glaucoma Service The Rabin Medical Center, Petach Tiqva, Israel

🇮🇱

Kaplan Medical Center, Rehovot, Israel

🇧🇪

UZ Leuven, Leuven, Belgium

and more 47 locations
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