Phase 3b Taltz–Zepbound Combo Drives 64% Relative ACR50 Gain; AI Biologics Pact with Chai Discovery
Phase 3b TOGETHER-PsA trial combining Taltz and Zepbound achieved a 31.7% ACR50 response vs. 0.8% for Taltz alone, marking a 64% relative increase. Lilly partnered with Chai Discovery to deploy its frontier AI platform and train an exclusive model on proprietary data to accelerate early-stage biologics discovery.
1. Eli Lilly Anchors Major Radiopharmaceutical Venture’s IPO
Eli Lilly stepped in as the anchor investor for Aktis Oncology’s initial public offering, underpinning a $318 million raise that underscores Lilly’s commitment to targeted radiopharmaceuticals. The agreement, struck in late 2025, gives Lilly the right to collaborate on Aktis’s proprietary miniprotein platform in a partnership valued at up to $1.2 billion. This strategic investment expands Lilly’s footprint in alpha-emitting therapies for solid tumors and positions the company to leverage Aktis’s actinium-225 and bismuth-213 candidates against Nectin-4 and B7-H3 targets. Investors view the deal as a signal that Lilly is accelerating its oncology pipeline diversification into novel radioconjugate approaches.
2. Collaboration with Chai Discovery to Accelerate AI-Driven Biologics
In January 2026, Lilly announced a multi-year collaboration with Chai Discovery to co-develop AI-designed biologic therapeutics. Under the agreement, Chai will build bespoke machine-learning models trained on Lilly’s proprietary datasets to drive zero-shot antibody and peptide design. The partnership follows Chai’s $230 million Series B financing, which valued the startup at $1.3 billion. Lilly intends to apply Chai’s technology to multiple immuno-oncology and metabolic targets, aiming to slash discovery timelines from months to weeks. Financial terms include an upfront payment and tiered development milestones, positioning Lilly to capture significant royalty streams on any candidate that advances to clinical proof-of-concept.
3. Phase 3b Trial Shows Dual Zepbound and Taltz Improves Psoriatic Arthritis and Weight Outcomes
Lilly reported positive data from the TOGETHER-PsA study combining tirzepatide with ixekizumab in patients with psoriatic arthritis and obesity. The dual regimen achieved a 31.7% response rate at 24 weeks versus 0.8% for ixekizumab alone on the primary composite endpoint, representing a 64% relative improvement in ACR50 measures. Average weight loss in the combination arm exceeded 10% of baseline body weight, compared with under 1% for monotherapy. Adverse events were predominantly mild to moderate gastrointestinal and injection-site reactions, consistent with known safety profiles. Management guided that these results could expand the clinical use of tirzepatide beyond metabolic indications and drive additional market penetration for both brands.