Allergan, an AbbVie Company, Announces Positive Phase 3 Topline Results for Investigational AGN-190584 for the Treatment of Presbyopia

Rhea-AI Summary

Allergan, a subsidiary of AbbVie (NYSE: ABBV), announced that the Phase 3 GEMINI 1 and 2 clinical trials for AGN-190584 (pilocarpine 1.25%) successfully met their primary endpoints, demonstrating significant improvement in vision for presbyopia patients. The studies involved 750 participants who received the treatment daily for 30 days. Results indicated a notable increase in near vision without compromising distance vision. The company plans to submit a New Drug Application to the FDA in the first half of 2021.

Positive

• Phase 3 GEMINI trials met primary efficacy endpoints.
• Statistically significant improvement in near vision for presbyopia patients.
• No serious adverse events reported.
• Potential additional treatment option for 128 million U.S. presbyopia sufferers.

Negative

• None.

NORTH CHICAGO, Ill., Oct. 28, 2020 /PRNewswire/ -- Allergan, an AbbVie (NYSE: ABBV) company, today announced the Phase 3 GEMINI 1 and 2 clinical trials evaluating the efficacy, safety and tolerability of investigational AGN-190584 (pilocarpine 1.25%) ophthalmic solution for the treatment of symptoms associated with presbyopia, met their primary efficacy endpoint. Additional details of these studies will be presented at future medical meetings and will serve as the basis for the New Drug Application submission to U.S. Food and Drug Administration (FDA) in the first half of 2021.

In GEMINI 1, the primary endpoint was met with a statistically significant greater proportion of participants treated with AGN-190584 who gained three lines (the ability to read three additional lines on a reading chart) or more in mesopic (in low light), high contrast, binocular Distance Corrected Near Visual Acuity (DCNVA) at Day 30, Hour 3 versus the vehicle (placebo). In GEMINI 2, the primary endpoint was also met with a statistically significant greater proportion of participants treated with AGN-190584 who gained three lines or more in mesopic, high contrast, binocular DCNVA without loss of greater than five letters in Corrected Distance Visual Acuity (CDVA) with the same refraction at Day 30, Hour 3 versus the vehicle. Further details including additional efficacy and safety results are included in the "About the Studies" section below.  

Roughly 128 million people in the U.S. experience presbyopia, a common and progressive eye condition that reduces the eye's ability to focus on near objects and usually impacts people after age 40. Results from a survey of 1,339 respondents, age 40-55, found that 90% were frustrated or irritated with presbyopia.

"Presbyopia symptoms can significantly disrupt everyday activities like reading, using a smartphone, working, and cooking," said George O. Waring IV, M.D., FACS, medical director, Waring Vision Institute, South Carolina. "While individuals currently have several options to help manage presbyopia, including glasses, contact lenses and surgery, research has shown that the majority of presbyopic individuals are frustrated with the use of contact lenses or glasses. These GEMINI findings support the possibility of another treatment option for people living with presbyopia."

In a non-presbyopic eye, the clear lens behind the iris can change shape and focus light to the retina, making it easier to see things up close. In a presbyopic eye, the clear lens hardens and does not change shape as easily, making it difficult to focus on near objects. AGN-190584 is an investigational eye drop designed to treat symptoms of presbyopia and is instilled in both eyes.

"Our research shows that the symptoms associated with presbyopia can significantly impact people's daily lives," said Michael R. Robinson, M.D., vice president, global therapeutic area head, ophthalmology, AbbVie. "The positive results from the GEMINI studies show the potential of this investigational optimized formulation of pilocarpine 1.25% to treat symptoms associated with presbyopia."

About the Studies
GEMINI 1 and 2 enrolled a total of 750 patients randomized in a one-to-one ratio of vehicle (placebo) to AGN-190584 (pilocarpine 1.25%). AGN-190584 was administered bilaterally, once-daily, for 30 days in both GEMINI 1 and 2 participants with presbyopia. In the GEMINI studies, AGN-190584 demonstrated significant near vision gains in mesopic (in low light) conditions without a loss of distance vision. There were no treatment emergent serious adverse events observed in any AGN-190584 treated participants. The most common treatment emergent non-serious adverse events occurring at a frequency of ≥3% in AGN-190584 treated participants were headache, conjunctival hyperaemia, vision blurred, and eye pain. In both studies, the primary endpoint was met. The majority of secondary endpoints were also met in both studies, including a significant improvement in patient-reported outcomes (PROs) such as an increase in vision-related reading ability, and reductions in the impact of presbyopia on daily life and use of coping behaviors to manage presbyopia.

About AGN-190584
AGN-190584 is an investigational optimized formulation of pilocarpine, a cholinergic muscarinic receptor agonist, that is being investigated for treating symptoms associated with presbyopia as a topical, once-daily drop delivered by a proprietary vehicle.

The proposed mechanism of action of AGN-190584 is through dynamic pupil modulation, an effect in which the iris sphincter is contracted to achieve pupil size reduction in an optimal range. The goal of this pupil size reduction is to increase depth of focus. Secondarily, it is believed to allow for increased accommodation through mild contraction of the ciliary muscle.

About Allergan Eye Care
As a leader in eye care, Allergan has discovered, developed, and delivered some of the most innovative products in the industry for more than 70 years. Allergan has launched over 125 eye care products and invested billions of dollars in new treatments for the most prevalent eye conditions, including glaucoma, ocular surface disease, and retinal diseases such as diabetic macular edema and retinal vein occlusion.

About AbbVie
AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com/. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions, among others, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those indicated in the forward-looking statements. Such risks and uncertainties include, but are not limited to, failure to realize the expected benefits from AbbVie's acquisition of Allergan plc ("Allergan"), failure to promptly and effectively integrate Allergan's businesses, competition from other products, challenges to intellectual property, difficulties inherent in the research and development process, adverse litigation or government action, changes to laws and regulations applicable to our industry and the impact of public health outbreaks, epidemics or pandemics, such as COVID-19. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2019 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its subsequent Quarterly Reports on Form 10-Q. AbbVie undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.

 

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SOURCE AbbVie

FAQ

What is the purpose of the GEMINI 1 and 2 trials for ABBV?

The GEMINI 1 and 2 trials evaluate the efficacy and safety of AGN-190584 in treating symptoms associated with presbyopia.

What were the key results from the Phase 3 GEMINI trials?

Both trials met their primary endpoints, showing significant improvements in near vision without loss in distance vision.

When does AbbVie plan to submit the New Drug Application for AGN-190584?

AbbVie plans to submit the New Drug Application to the FDA in the first half of 2021.

How many participants were involved in the GEMINI trials?

The GEMINI trials enrolled a total of 750 patients.

What percentage of U.S. adults are affected by presbyopia?

Approximately 128 million people in the U.S. experience presbyopia.