Merck Presents One-Year Results from the Pivotal Phase 2b/3 BRUNELLO Study Evaluating Remigromig, a Tri-specific Agonist of the Wingless-related Integration Site (Wnt) Pathway, in Adults with Diabetic Macular Edema at AAO 2026

Merck (MRK) reported one-year results from its BRUNELLO trial for remigromig, an investigational drug for diabetic macular edema (DME). Both doses met the primary endpoint, showing non-inferiority to ranibizumab in visual acuity improvement. However, adverse events related to proliferative diabetic retinopathy were more frequent with remigromig. Merck plans to discuss results with regulators and is conducting further analyses.

Merck (MRK) reported that its investigational drug, remigromig, met the primary endpoint of non-inferiority in visual acuity compared to ranibizumab in a trial for diabetic macular edema. The BRUNELLO trial enrolled 984 participants, with mean visual acuity gains of 9.1 and 8.7 letters for remigromig doses, versus 11.8 for ranibizumab. Adverse events were higher with remigromig. Merck plans to discuss the results with regulators.

Merck's experimental eye drug, remigromig, met its primary endpoint in a Phase 2b/3 trial for diabetic macular edema (DME), showing non-inferior visual acuity compared to ranibizumab. However, it had a higher rate of adverse events related to proliferative diabetic retinopathy. The company plans to discuss the results with regulators and continue evaluating the drug in ongoing studies.

Merck (MRK) presented one-year results from the BRUNELLO trial for remigromig, a biologic targeting the Wnt pathway for diabetic macular edema (DME). Remigromig met non-inferiority in visual acuity compared to ranibizumab, with mean gains of +9.1 and +8.7 letters for 0.5 mg and 0.8 mg doses, respectively, versus +11.8 letters for ranibizumab. Adverse events related to proliferative diabetic retinopathy were more frequent with remigromig.

Merck Animal Health, a division of Merck & Co. (MRK), announced peer-reviewed studies on gilvetmab, an anti-PD-1 monoclonal antibody for canine cancer treatment. The studies showed efficacy in melanoma and mast cell tumors, with a 66.7% clinical benefit rate. Gilvetmab is conditionally approved by the USDA and available in the U.S. The company plans further studies to support its safety and efficacy.

A new NIH initiative to accelerate personalized cancer vaccine development has sparked a rally in biotech stocks. Moderna, Novavax, BioNTech, Pfizer, Merck, and Vaxcyte saw gains. The program, launching in December, focuses on pancreatic, liver, colorectal cancers, and childhood tumors. Moderna and Merck reported positive Phase 3 results for their mRNA cancer vaccine in August. BioNTech is advancing multiple cancer therapies.