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Will the FDA approve VERVE-102?
The odds
- Before 203583%
- Before 203479%
- Before 203375%
- Before 203272%
- Before 203165%
- Before 203054%
How the odds have moved
Before 2035: 83% on Oct 20, 83% now.
Each outcome's chance over time on Kalshi. The dots along the bottom are headlines about its subject: point at one to read it.
Every outcome
| Outcome | Chance | Day | Bid | Ask | Pays | Contracts |
|---|---|---|---|---|---|---|
| Before 2035 | 83% | 79¢ | 87¢ | $1.15 | 332 | |
| Before 2034 | 79% | 77¢ | 81¢ | $1.23 | 48.00 | |
| Before 2033 | 75% | 71¢ | 79¢ | $1.27 | 2.00 | |
| Before 2032 | 72% | 68¢ | 76¢ | $1.32 | 35.00 | |
| Before 2031 | 65% | 61¢ | 69¢ | $1.45 | 117 | |
| Before 2030 | 54% | 50¢ | 57¢ | $1.75 | 1.2K |
"Pays" is what a $1 stake returns if that outcome happens, at the price shown (before any fees). Bid and ask are the best prices to sell and buy "Yes".
The news: FDA, VERVE
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Alice Eve Signs With Verve, Boards Indie 'The Long Run'EXCLUSIVE: Actress Alice Eve has inked with Verve and lined up a new project: a grief-themed indie called The Long Run that’s slated for production this fall. In The Long Run, Eve plays Claire Stanton, a woman shattered by the loss of her… -
The FDA says there’s no estrogen patch shortage. Women are struggling to fill prescriptions.Estrogen patches are the most commonly reported shortage in the U.S., but the FDA says it’s working to boost supply. Women across the country are still struggling to fill prescriptions for estrogen patches. -
FDA issues recall over compounded GLP-1 weight loss drugsFox News contributor Dr. Stephanie Widmer discusses the recall of certain compounded GLP-1 medications over sterility concerns. FDA issues recall over compounded GLP-1 weight loss drugs Fox News contributor Dr. Stephanie Widmer discusses… -
FDA has finalized its guidance on apps related to drugsSTAT is a media company focused on finding and telling compelling stories about health, medicine, and scientific discovery. We produce daily news, investigative articles, and narrative projects in addition to multimedia features, podcasts… -
FDA to pull common but ineffective cold medicine from marketNovember 7, 2024 / 12:32 PM EST / CBS News The Food and Drug Administration announced Wednesday that it would seek to pull a widely used ingredient in cough and cold medicines from the market, after the agency's scientists concluded that… -
MDMA-assisted therapy could get FDA approval as soon as January, top advocate predicts — but there’s a major problem loomingA drug once synonymous with rave culture could soon be making its way into a very different setting: the therapist’s office. A leading psychedelics advocate is “very optimistic” the Food and Drug Administration could approve MDMA-assisted… -
Telehealth leapfrogs FDA approval with off-label GLP-1 prescriptions for addictionSTAT Telehealth leapfrogs FDA approval with off-label GLP-1 prescriptions for addiction Online platforms, experts say, can shift the burden of vetting unapproved drugs on to patients Katie covers the impact of health technology on… -
Nasal decongestant phenylephrine, found in many over-the-counter cold and allergy medicines, doesn't work, FDA experts sayUpdated on: September 16, 2023 / 8:59 PM EDT / AP The leading decongestant used by millions of Americans looking for relief from a stuffy nose is likely no better than a dummy pill, according to government experts who reviewed the latest… -
Verve Display invests in swissQprint Nyala 5Verve Display has become the latest print and display specialist to invest in the swissQprint Nyala 5, after conducting a range of print tests using its most challenging files, colours, and gradients Experiential display specialist, Verve… -
20 years after fatal hit-and-run, loved ones of Pete Ververs still looking for answersMarion, N.Y. (WHAM) — "They left a person in the middle of the road," Tom Chopan told 13WHAM on Oct 22, 2006. " Not just a person, my friend and a future father." 20 years ago, those words captured the pain of a friend trying to make sense… -
Recent FDA Actions: Spring 2023In breast cancer, approval for elacestrant and a new indication for sacituzumab govitecan; approval for pirtobrutinib for mantle cell lymphoma. The primary end point in the study was PFS, and secondary end points included OS, overall… -
FDA approves ‘breakthrough’ melanoma drugThe Food and Drug Administration has granted accelerated approval to pembrolizumab (Keytruda, Merck) for treatment of advanced or unresectable melanoma in patients who have stopped responding to other drugs. The five prior FDA approvals…
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Odds are traders' prices on Kalshi, Polymarket, ForecastEx and Crypto.com, not forecasts by 4Search. Prices read from the venues 3 min ago. Prices may be delayed. Money traded on Kalshi and ForecastEx is estimated from contracts. Not betting or investment advice.
Prediction-market prices are what traders pay for each outcome on Kalshi, Polymarket, ForecastEx and Crypto.com, read as the market's implied chance. They are not forecasts by 4Search, can move fast and can be wrong; they are read every few minutes and may be delayed. Money traded on Kalshi and ForecastEx is estimated from contracts at their price. News comes from the 4Search index; prices of stocks, rates and coins from 4Search Finance. Nothing here is betting, financial or investment advice. Terms of use.