Posts Tagged ‘Latisse’

Answers to Your Latisse Eyelash Enhancement Questions

Monday, January 4th, 2010

Q: What is Latisse?

A: Latisse is a bimatoprost ophthalmic solution 0.03%, originally latisse-phoenix-tucsondeveloped and used as a glaucoma medication. In using the medication, many patients noticed that their eyelashes grew. Some even had to trim their lashes due to excessive length. Allergan, who owned the medication, began to market it as Latisse, for topical use in patients with “inadequate eyelashes.”

Q: How long has Latisse been on the market?

A: Although Latisse has been available for just over 6 months, its related safety record as an eye drop solution, spans over 10 years. Any medication that is used in the eye must be very safe.

Q: Why do I need a prescription for Latisse?

A: Latisse is not an over-the-counter medication. The FDA approved Latisse as a prescription medication to treat hypotrichosis, i.e. reduced amount of eyelash growth.  Using Latisse can result in eyelash improvement of 105% in thickness and over 25% in length.

Q: How does Latisse work?

A: Latisse is thought to affect the growth stage of eyelashes by increasing the duration of the growth phase while increasing the number of hairs in the growth phase.

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How Allergan Brought Latisse Eyelash Enhancement to Arizona

Thursday, June 25th, 2009

Sometimes new drugs make their way to the market inadvertently and become popular for uses that were never originally intended; such is the case with Allergan’s new eyelash enhancer, Latisse. 

Latisse was born out of a group of popular medications called topical prostaglandins, drugs frequently used to decrease intra-ocular pressure in glaucoma patients. What was first labeled a ‘complication’ or side effect of using prostaglandins was “hypertrichosis,” a condition characterized by darker, fuller eyelashes.   

 Allergan offered the topical prostaglandin Lumigan in 2001, a drug containing an important ingredient called bimatoprost. Two important precursors to Latisse occurred once the FDA gave its clearance to Lumigan.

  • Jan Marini Skin Research Inc had over $2 million worth of product seized by the Food and Drug Administration.  The product, Age Intervention Eyelash, evidently contained bimatoprost, which was unapproved for cosmetic use at the time. Allergan later filed a patent infringement suit against Jan Marini and several other companies that had tried to market bimatoprost in their eyelash enhancing drugs.
  • Some doctors started prescribing Lumigan off-label to enhance eyelashes.  Knowing the desirable side effects it could produce. But Lumigan wasn’t formulated for cosmetic use and many believed more research was needed to confirm the safety of topical prostaglandins for cosmetic use.  

Research and clinical trials are exactly what Alllergan did.  In one early study, 278 healthy adults with minimal to moderate eyelash prominence applied bimatoprost or a placebo to their lash line.  The results were favorable; researchers observed that the average patient’s eyelashes were 25 percent longer, 106 percent fuller, and 18 percent darker, while only 3.6 percent experienced itchy eyes and redness, and only 2.9 percent experienced skin hyperpigmentation.  

Latisse received FDA approval late last year for the treatment of ‘inadequate’ eyelashes.  Allergan now owns the patent on use of bimatoprost for eyelash enhancement.

Contact the office of Dr. Mikel Lo for more information on Latisse in Arizona.