Resolution criteria on PolyGram: Retatrutide is a triple agonist hormone/peptide drug developed by Eli Lilly and currently in trial to treat obesity, fatty liver disease, type-2 diabetes, knee osteoarthritis, and more. This market will resolve to "Yes" if the U.S. Food and Drug Administration (FDA) grants a full or conditional approval for Eli Lilly’s for a drug product whose active ingredient is Eli Lilly’s retatrutide (including any brand name or identifier such as LY3437943) for any use between market creation and December 31, 2026, 11:59 PM ET.
PolyGram is an on-chain prediction market where you trade YES or NO outcome shares with real USDC on Polygon. For this market, buy YES if you believe the event will happen, or NO if you think it won't. Your maximum loss is your stake — winning shares pay $1.00 each at resolution. Unlike sportsbooks, there is no house edge: prices are set by supply and demand from other traders and reflect the crowd's real-time probability.
Market outcomes
| FDA approves Retatrutide this year? | 21% YES | 79% NO |
Eli Lilly's retatrutide, a triple GLP-1/GIP/glucagon receptor agonist, is currently in late-stage clinical development for obesity, type-2 diabetes, and fatty liver disease. The FDA approval question hinges on whether Lilly completes its regulatory submission and receives a green light by end-2026. The 21% implied probability on Polymarket's order book reflects meaningful uncertainty around both the timeline and the regulatory pathway, with traders pricing in the possibility of delays, additional data requests, or a decision extending into 2027.
Comparable precedent matters here. Tirzepatide (Mounjaro), Lilly's dual GLP-1/GIP agonist, moved from Phase 3 completion to FDA approval in roughly 18 months. However, retatrutide's triple mechanism and broader indication portfolio—spanning metabolic disease and osteoarthritis—may require more extensive safety and efficacy data. Semaglutide's obesity indication took approximately two years from Phase 3 readout to approval. The current 21% probability suggests the market views a 2026 approval as plausible but not baseline.
Key catalysts include Phase 3 readout announcements, which typically precede FDA submissions by months. Lilly's recent earnings calls and investor updates have indicated Phase 3 data expected in 2024–2025 for various indications. A successful readout would likely accelerate the probability upward; conversely, any safety signals or efficacy shortfalls would compress it. The regulatory pathway—whether Lilly pursues breakthrough designation or standard review—will also influence timeline expectations. Traders should monitor Lilly's quarterly guidance and FDA meeting minutes for signals on submission timing.
The Food and Drug Administration (FDA) is a federal agency of the United States Department of Health and Human Services (HHS). The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (m
Resolution is handled by the UMA optimistic oracle on Polygon. A proposer submits the outcome, a two-hour dispute window opens, and if no one stakes a counter-claim the payout is final. Contested outcomes escalate to UMA token-holder voting. Payouts clear in USDC to the winning side.
The mechanics for trading "FDA approves Retatrutide this year?" are the same as any other PolyGram event contract. Each YES share resolves to $1 if the event happens, or $0 if it doesn't. The current price between 0¢ and 100¢ is the market's probability estimate, set live by the order book.
$563K in lifetime turnover and $2K of resting liquidity puts this market in the top 2% by volume for drug contracts on PolyGram. Order-book depth is thin — large orders may need to be split across the book or executed as limit orders.
The market has been open for 4 months — the price has had time to stabilise as new information arrived.
Higher-volume markets tend to have tighter spreads and faster price discovery — meaning the displayed YES/NO percentages are more likely to reflect the true crowd-implied probability rather than a single trader's directional view.
As of today, traders on Polymarket price this outcome at 21%. The number updates continuously as the order book clears. PolyGram mirrors the same live odds with locale-aware formatting and USDC settlement.
Resolution is handled by the UMA optimistic oracle on Polygon. A proposer submits the outcome, a 2-hour dispute window opens, and if uncontested the payout is final. Contested outcomes escalate to UMA token holders.
This prediction market is scheduled to close on 31 December 2026. After the resolving event occurs, settlement typically clears within 24 hours once the UMA optimistic oracle confirms the outcome. All payouts are in USDC on the Polygon network.
To trade on this prediction market, create a free PolyGram account at polygram.ink, deposit USDC via Polygon, and place a YES or NO order on the outcome you believe in. You can learn more on our how-it-works page. Your maximum loss is limited to your stake — there is no leverage or margin.
When the outcome is determined, winning YES shares pay out $1.00 each in USDC, while losing shares pay $0. Settlement is handled by the UMA optimistic oracle on Polygon — a proposer submits the result, a two-hour dispute window opens, and if uncontested, payouts are distributed automatically. You can withdraw your winnings to any Polygon wallet.
Prediction-market positions can lose 100% of staked capital. Outcomes are uncertain by definition — historical accuracy of crowd-implied probabilities is high in aggregate but not for any single market. PolyGram does not provide investment advice. Trade only with capital you can afford to lose.
Regulatory status varies by jurisdiction. Germany, the United States, and most EU countries treat Polymarket-style event contracts under one of three frameworks: financial derivative, gambling product, or unregulated novel asset. Consult local counsel before trading.
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