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Vision Loss Reduction with Avacincaptad Pegol for Geographic Atrophy: A 12-Month Post Hoc Analysis of the GATHER1 and GATHER2 Trials.
Danzig, Carl J; Khanani, Arshad M; Kaiser, Peter K; Chang, Margaret A; Kovach, Jaclyn L; Lally, David R; Rachitskaya, Aleksandra; Sheth, Veeral S; Vajzovic, Lejla; Clark, Julie; Tang, Justin; Zhu, Liansheng; Desai, Dhaval; Chakravarthy, Usha.
Affiliation
  • Danzig CJ; Rand Eye Institute, Deerfield Beach, Florida; Florida Atlantic University, Charles E. Schmidt School of Medicine, Boca Raton, Florida.
  • Khanani AM; Sierra Eye Associates, Reno, Nevada; University of Nevada, Reno School of Medicine, Reno, Nevada.
  • Kaiser PK; Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
  • Chang MA; Retinal Consultants Medical Group, Sacramento, California.
  • Kovach JL; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.
  • Lally DR; New England Retina Consultants, Springfield, Massachusetts.
  • Rachitskaya A; Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
  • Sheth VS; University Retina, Chicago, Illinois.
  • Vajzovic L; Duke University Eye Center, Durham, North Carolina.
  • Clark J; Iveric Bio, an Astellas Company, Parsippany, New Jersey.
  • Tang J; Iveric Bio, an Astellas Company, Parsippany, New Jersey.
  • Zhu L; Iveric Bio, an Astellas Company, Parsippany, New Jersey.
  • Desai D; Iveric Bio, an Astellas Company, Parsippany, New Jersey.
  • Chakravarthy U; Queen's University of Belfast, Royal Victoria Hospital, Belfast, United Kingdom. Electronic address: u.chakravarthy@qub.ac.uk.
Ophthalmol Retina ; 2024 May 07.
Article in En | MEDLINE | ID: mdl-38719191
ABSTRACT

PURPOSE:

To evaluate the impact of reduction in geographic atrophy (GA) lesion growth on visual acuity in the GATHER trials using categorical outcome measures.

DESIGN:

Randomized, double-masked, sham-controlled phase 3 trials.

PARTICIPANTS:

Aged ≥50 years with noncenter point-involving GA and best-corrected visual acuity (BCVA) of 25 to 80 ETDRS letters in the study eye.

METHODS:

GATHER1 consisted of 2 parts. In part 1, 77 patients were randomized 111 to avacincaptad pegol (ACP) 1 mg, ACP 2 mg, and sham. In part 2, 209 patients were randomized 122 to ACP 2 mg, ACP 4 mg, and sham. In GATHER2, patients were randomized 11 to ACP 2 mg (n = 225) and sham (n = 223). A post hoc analysis of 12-month data for pooled ACP 2 mg and sham groups is reported. MAIN OUTCOME

MEASURES:

Proportion of study eyes that experienced ≥10-, ≥15-, or ≥20-BCVA ETDRS letter loss from baseline to month 12; time-to-event analysis of persistent vision loss of ≥10, ≥15, or≥ 20 BCVA letters from baseline at ≥2 consecutive visits over 12 months; proportion of study eyes with BCVA loss to a level below driving eligibility threshold at month 12 among those eligible to drive at baseline.

RESULTS:

Lower proportions of study eyes experienced ≥10-, ≥15-, or ≥20-BCVA letter loss from baseline over 12 months with ACP 2 mg (11.6%, 4.0%, and 1.6%, respectively) versus sham (14.1%, 7.6%, and 4.5%, respectively). There was a reduction in the risk of persistent loss of ≥15 BCVA ETDRS letters with ACP 2 mg (3.4%) versus sham (7.8%) through 12 months. A lower proportion of study eyes treated with ACP 2 mg reached the threshold for driving ineligibility versus sham by 12 months.

CONCLUSIONS:

Treatment with ACP 2 mg delayed the risk of progression to persistent vision loss (i.e., ≥10-, ≥15-, and ≥20-BCVA letter loss or BCVA loss to a level below driving eligibility threshold) versus sham over 12 months. FINANCIAL DISCLOSURE(S) Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Retina Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Retina Year: 2024 Document type: Article Country of publication: