Manifold MarketsGeen KYCGeverifieerde afwikkelingsgegevensRedelijk gekalibreerdHuidige gemeenschapsvoorspellingNee 68.1%
Voorspellers
6
Vraagtype
binary
Methodologie
Play-money forecasting platform
Brontype
Voorspelling
Marktdata
Bijgewerkt 17 uur geleden
Verouderd4 sep 25, 22:10 UTC31 dec 29, 23:59 UTC
Trends
Gerelateerde Markten
Gerelateerde vragen voor context, geen vergelijking van gelijkwaardige contracten.
Will MDMA-assisted therapy for PTSD be approved by the FDA before 2030?
Manifold MarketsWill a vaccine for HIV be approved by the FDA by 2030?
Manifold MarketsWill a vaccine for HIV be approved by the FDA and be available for public use by 2027?
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FutuurTdi-11861 (a fast-acting male contraceptive) approved for human clinical trials by the end of 2026?
FutuurOrion (a device that promises to project artificial vision into the brains of blind people) approved for sale by the end of 2027?
FutuurRegels
Resolution criteria
- Resolve YES if, by 11:59:59 pm Eastern Time on December 31, 2029, the U.S. FDA grants any marketing authorization for human use (approval, licensure, De Novo grant, or 510(k) clearance) to a product that fits this definition: a living, multicellular construct assembled ex vivo from animal or human cells, engineered to perform autonomous tasks in vivo (e.g., locomotion/drug delivery)—i.e., a “xenobot/biobot/anthrobot”-type product.
- Verification must appear in one of the FDA’s public databases: Drugs@FDA (NDAs/BLAs), Purple Book (licensed biologics), PMA, De Novo, or 510(k).
- Links: Drugs@FDA, Purple Book, PMA, De Novo, 510(k).
- (fda.gov, accessdata.fda.gov)
- EUAs, INDs/IDEs, in vitro–only/research-use-only authorizations, animal-use approvals, or products consisting solely of dissociated cells or live microbes (e.g., standard cellular therapies or live biotherapeutics) do NOT count.
Open markten
Health & Medicine
POLYMARKETHantavirus pandemic in 2026?
- No-0.1pt97%
- Yes+0.1pt3%
- Totaal volume
- € 15,6 mln.
- 24u volume
- € 18,3K
KALSHIWill WHO declare Hantavirus a Public Health Emergency of International Concern this Year?
- No96%
- Yes+1.9pt4%
- Totaal volume
- € 1,6 mln.
- 24u volume
- € 5,2K
KALSHIWhen will Intellia Therapeutics submit a BLA for Lonvo-z?
- before October+64.0pt98%
- before 2027+22.0pt98%
- before December+30.0pt98%
+3 extra uitkomsten
POLYMARKETFDA approves skin cancer vaccine by which date?
- December 31,+6.0pt65%
- September+2.0pt41%
- June28%
- Totaal volume
POLYMARKETNew pandemic in 2026?
- No+0.5pt94%
- Yes-0.5pt6%
- Totaal volume
- € 916K
- 24u volume
- € 1,5K
KALSHIMeasles cases in 2026?
- Above 300099%
- Above 400097%
- Above 6000-2.0pt57%
+2 extra uitkomsten
- Totaal volume
- € 863,6K
- 24u volume
- € 1K
- Ebola pandemic in 2026?
- Will 3 mg THC beverages be federally legal to sell?
- Ebola pandemic in 2026?
- Measles cases in U.S. in 2026?
- FDA decision: Bepirovirsen by GlaxoSmithKline (in 2026)
- When will Heidi Overton be confirmed as Commissioner of the FDA?
- What will the average number of measles cases be during Trump's term?
- Will the FDA approve any psychedelic substance for medical use this year?
- When will the FDA reclassify BPC-157 to Category 1?
- FDA decision: Saroglitazar by Zydus Therapeutics (in 2026)
- Will the FDA approve CagriSema?
Veelgestelde vragen
- Wat zijn de huidige kansen voor Will Xenobots Be Approved By The FDA Before 2030??
- Manifold Markets prijst No op 68% per 8 september 2026.
- Wanneer wordt Will Xenobots Be Approved By The FDA Before 2030? afgewikkeld?
- Will Xenobots Be Approved By The FDA Before 2030? wordt naar verwachting op 31 december 2029 afgewikkeld.
- Hoe wordt Will Xenobots Be Approved By The FDA Before 2030? afgewikkeld?
- Manifold Markets wikkelt deze markt als volgt af: Resolution criteria