Resolution criteria on PolyGram: As of market creation, the FDA's expected decision date for the specified application is May 10, 2026. This market will resolve to "Yes" if the U.S. Food and Drug Administration (FDA) grants full or conditional approval for argenx's Vyvgart as a treatment for seronegative generalized myasthenia gravis by May 24, 2026, 11:59 PM ET. Otherwise, this market will resolve to "No." An approval is defined as: For new drugs: FDA issuance of an approval letter for a New Drug Application (NDA) or Biologics License Application (BLA) For already-marketed drugs seeking new indications: FDA approval of a supplemental NDA (sNDA) or supplemental BLA (sBLA) for the specific indication referenced For generic…
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 argenx's Vyvgart? | 100% YES | 0% NO |
The FDA is scheduled to decide on argenx's application to expand Vyvgart's indication to seronegative generalised myasthenia gravis (gMG) by 10 May 2026. Vyvgart (efgartigimod) is already approved for seropositive gMG, having received FDA clearance in December 2021. The current application seeks to extend use to seronegative patients, who represent roughly 10–15% of the gMG population. The 100% implied probability on Polymarket's order book reflects market confidence in approval, though this represents a compressed risk assessment given the compressed timeline and the precedent of the drug's existing safety and efficacy profile in the seropositive indication.
Regulatory precedent suggests high approval likelihood. The FDA has historically approved indication expansions for monoclonal antibodies and complement inhibitors targeting autoimmune conditions when clinical data demonstrate efficacy in new patient subsets. Argenx's Phase 3 trial data for seronegative gMG, presented at major neurology conferences, showed statistically significant improvements in muscle strength measures. The company's track record with the seropositive indication and established manufacturing infrastructure reduce regulatory friction compared to novel drug applications.
Key catalysts include any FDA communications requesting additional data before the decision date, which would signal potential delays beyond May 2026. Traders should monitor argenx's quarterly earnings calls and clinical updates for any mention of FDA interactions. The settlement window extends to 24 May 2026, allowing a two-week buffer beyond the expected decision date for administrative processing. Approval timing could shift if the FDA issues a complete response letter requesting supplemental data, though current market pricing suggests traders assess this risk as minimal.
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 argenx's Vyvgart?" 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.
$10K in lifetime turnover and $0 of resting liquidity puts this market in the below the median 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 under a month — fresh enough that information asymmetry remains a real factor.
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 100%. 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 10 May 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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