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FDA decision: Bepirovirsen by GlaxoSmithKline (in 2026)
Settled YesA day before, traders gave it 95%.
The last odds before it closed
How the odds have moved
Yes: 96% on Oct 20, 95% 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 | Last odds | Day | Bid | Ask | Pays | Contracts |
|---|---|---|---|---|---|---|
| ✓ Yes | 95% | 4.2K |
"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, Bepirovirsen, GlaxoSmithKline
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FDA Approves Bepirovirsen, First Antisense Therapy for Chronic Hepatitis BThe FDA approved bepirovirsen (Hibsago; GSK) with nucleos(t)ide analogue therapy for chronic hepatitis B, based on B-Well 1 and 2 functional cure rates of 19% vs 0% with placebo. The FDA approved Hibsago (bepirovirsen; GSK), the first… -
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 Approves Bepirovirsen Injection to Treat Chronic Hepatitis BApproval was given to GSK, making its product the first antisense oligonucleotide established for the treatment of chronic hepatitis B. The FDA approved GSK’s bepirovirsen (Hibsago) injection for the treatment of hepatitis B virus (HBV)… -
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 Approves Bepirovirsen for Chronic Hepatitis BThe US Food and Drug Administration (FDA) has approved bepirovirsen (Hibsago), the first FDA-approved antisense oligonucleotide for chronic hepatitis B virus (HBV) infection, for use alongside existing antiviral therapy in certain adults… -
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… -
GlaxoSmithKline to sell business to Japanese firmThe board of directors of GlaxoSmithKline Consumer Nigeria (GSK) Plc has accepted a binding offer from a Japanese firm, Suntory Beverage & Food Nigeria Limited, a subsidiary of Suntory Beverage and Food Limited (SBF) for the divestment of… -
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… -
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… -
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 Subcutaneous Risankizumab Induction for Crohn’s DiseaseApproval rests on the phase 3 AFFIRM trial, in which 56% of patients reached clinical remission at week 12 vs 30% with placebo. The US Food and Drug Administration (FDA) approved a subcutaneous induction regimen of risankizumab-rzaa…
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Odds are traders' prices on Kalshi, Polymarket, ForecastEx and Crypto.com, not forecasts by 4Conservative. Prices read from the venues 4 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 4Conservative, 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 4Conservative index; prices of stocks, rates and coins from 4Conservative Finance. Nothing here is betting, financial or investment advice. Terms of use. How to use Predictions