Evidence map›Paper›PMID 42718940›Full record

ArticleOphthalmology science2026

GOLDEN: Efficacy and Safety of Complement Factor B Antisense, Sefaxersen, in Geographic Atrophy due to Age-Related Macular Degeneration.

Glenn J Jaffe, Charles C Wykoff, Michael L McCaleb, Terrance D Barrett, Ashely Frazer-Abel, Daniel Norris, Ulrich F O Luhmann, Cathy Cukras, Lixuan Yin, Mark Lomax and 4 more

Abstract read
In one paragraph

Article in Ophthalmology science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Glenn J JaffeDuke University School of Medicine, Durham, North Carolina.
Charles C WykoffRetina Consultants of Texas, Houston, Texas.
Michael L McCalebIonis Pharmaceuticals, Inc, Carlsbad, California.
Terrance D BarrettIonis Pharmaceuticals, Inc, Carlsbad, California.
Ashely Frazer-AbelExsera Biolabs, University of Colorado School of Medicine, Aurora, Colorado.
Daniel NorrisIonis Pharmaceuticals, Inc, Carlsbad, California.
Ulrich F O LuhmannF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Cathy CukrasHoffmann-La Roche Inc, Little Falls, New Jersey.
Lixuan YinIonis Pharmaceuticals, Inc, Carlsbad, California.
Mark LomaxRoche Products Ltd, Welwyn Garden City, United Kingdom.
Sascha FauserF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Eugene SchneiderIonis Pharmaceuticals, Inc, Carlsbad, California.
Gary T BriceIonis Pharmaceuticals, Inc, Carlsbad, California.
GOLDEN Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate the efficacy and safety of sefaxersen, an investigational antisense oligonucleotide targeting complement factor B (FB), in slowing the progression of geographic atrophy (GA) secondary to age-related macular degeneration (AMD). Design: Randomized, double-masked, placebo-controlled, adaptive phase II clinical trial. Subjects: A total of 332 patients with GA secondary to AMD were enrolled, with 91% of treated patients completing the final study visit at 56 weeks. Methods: In stage 1, 58 patients received subcutaneous injections of 40, 70, or 100 mg sefaxersen or placebo monthly. An interim analysis for FB, pharmacokinetics, and safety was conducted when patients reached at least 13 weeks of treatment to select 2 doses for expansion. In stage 2, an additional 274 patients were randomized to 40 or 70 mg sefaxersen or placebo. Patients were stratified based on baseline GA size, baseline rate of GA growth, and presence/history of exudative choroidal neovascularization in the fellow eye. Geographic atrophy area was assessed by fundus autofluorescence imaging. Safety assessments included ocular and systemic adverse events, laboratory parameters, and vital signs. Main Outcome Measures: The primary endpoint was the rate of GA lesion growth from baseline to week 49. Prespecified endpoints included changes from baseline in best-corrected visual acuity, low-luminance visual acuity, systemic complement measures, and occurrence of treatment-related adverse events. Results: Sefaxersen did not significantly reduce the rate of GA growth versus placebo. Differences in adjusted mean GA rate of growth versus placebo were -0.25 mm Conclusions: Sefaxersen reduced systemic FB levels and alternative pathway activity, but the effect on GA growth rate was not significant compared with placebo. The treatment was well tolerated with a safety profile consistent with previous studies. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

AMDAntisense therapeuticsComplementGeographic atrophy

Identifiers

PMID42718940
PMCPMC13553563

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.