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%
Closed: May 28, 8:00 PM EST
Polymarket
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.
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.