TOTAL VOLUME:

$134b

24H VOL:

$107,351,958

24H TRANSACTIONS:

2,388,728,490

OPEN INTEREST:

$1,416,970,024

400,720

Markets across

30,097

events

MATCHED EVENTS:

2,633

PLATFORM COVERAGE:

5

Polymarket:

39%

VS.

Kalshi:

61%

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FDA approves MannKind's Afrezza?
polymarket

FDA approves MannKind's Afrezza?

Volume:
$3,090

FDA approves MannKind's Afrezza?

 - Polymarket

FDA approves MannKind's Afrezza? - Polymarket

1W

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Vol.

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Resolved Jun 2, 2026

Closed: May 28, 8:00 PM EST

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FDA approves MannKind's Afrezza?

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100%
Yes 100¢No 0¢
0.1¢
N/A
$3,090
N/A
N/A
N/A
Settled
Yes
Total markets: 1

Intro

This market tracks whether the FDA will approve MannKind's Afrezza inhaled insulin for treating children and adolescents with type 1 or type 2 diabetes. On Polymarket, the probability of FDA approval stands at 57.0%. Resolution will be determined by official FDA communications or credible reporting, with the agency's expected decision date set for May 29, 2026. Watch for the FDA's action letter on or before the June 12, 2026 deadline to determine whether MannKind receives standard approval, accelerated approval, or conditional approval for this pediatric indication.

Frequently asked questions

The PredictionHero dashboard tracks real-time odds and trading activity for the FDA approval of MannKind's Afrezza on Polymarket. You can monitor the current implied probability that the FDA will approve Afrezza, updated continuously as traders buy and sell shares. The dashboard displays total market volume of $3,090 and 24-hour volume of $1,023, helping you gauge liquidity and recent interest. Price history charts show how market sentiment has evolved, revealing whether confidence in approval has grown or declined over time. This data enables informed decision-making on whether to trade for or against FDA approval.

Prediction market odds on Polymarket reflect real-money bets from traders and investors, often incorporating non-public signals and expert analysis faster than traditional forecasts. Analyst reports on MannKind's Afrezza typically focus on clinical trial data, regulatory feedback, and competitive positioning in the rapid-acting insulin market. Prediction markets aggregate dispersed knowledge into a single price, whereas analyst forecasts remain fragmented across institutions. When market odds diverge significantly from analyst consensus, it may signal either market inefficiency or that traders possess information analysts have not yet incorporated. Comparing both sources provides a more complete picture of approval likelihood.

The market resolves on May 29, 2026, at which point the outcome is determined by whether the FDA has issued an approval decision for MannKind's Afrezza. Resolution hinges on official FDA communications and regulatory filings. The event captures the binary outcome of approval or non-approval by the end date. Traders should monitor FDA announcements, advisory committee meetings, and MannKind press releases for signals of imminent decisions. Any regulatory action or formal approval letter before the deadline will trigger market settlement. After resolution, no further trading occurs on this contract.

Key catalysts include FDA advisory committee meetings, where experts review clinical and safety data on Afrezza; positive or negative committee votes typically move odds sharply. MannKind earnings calls and investor updates may reveal new regulatory feedback or timeline guidance. Competitive approvals in rapid-acting insulin could influence perceived market opportunity. Adverse event reports or safety concerns would reduce approval odds, while favorable clinical data or regulatory guidance would increase them. FDA action letters or requests for additional information would signal approval status. Industry news about MannKind's manufacturing or commercial readiness may also shift trader sentiment. Close monitoring of SEC filings and FDA correspondence helps anticipate major price moves.