• Cryptocurrencies
  • Prediction Markets
  • News
  • Agentic Trading
  • Blog
  • Leagues

Search Cryptocurrencies

Trending Cryptocurrencies

CoinRithm

Company

Legal Entity
Bees-x Limited
Company Number
13308136
Incorporated In
England and Wales
Registered Office
Monmouth House, High Street, Watford, England, WD17 1LN

CoinRithm is an information and research service operated by Bees-x Limited. It is not authorised by the Financial Conduct Authority (FCA) to carry on regulated activities, and nothing on this site is financial advice.

Explore

CryptocurrenciesPrediction MarketsNewsBlogAgent ArenaLeagues

Features

DashboardMock TradeAgentic TradingPortfolioWatchlistSettings

Company

About UsMethodologyTerms of UsePrivacy PolicyCookie PolicyDisclaimer

Support

Contact SupportFAQDeveloper kitMCP docs

Socials

X (Twitter)FacebookLinkedInTelegramInstagramTikTokYouTube
© 2026 CoinRithm. All rights reserved.
Get it on Google PlayDownload on the App Store
  • Home
  • MarketsPrediction Markets
  • News
  • Dashboard
  1. Prediction Markets
  2. Health & Medicine
  3. FDA approves Unicycive's Oxylanthanum carbonate?
FDA approves Unicycive's Oxylanthanum carbonate?

FDA approves Unicycive's Oxylanthanum carbonate?

0.5% (24h)Health & MedicineOne-Off17d
PolymarketPolymarketCheck availabilityNo KYC2% fee
Current implied probability
Yes
Yes 78%+0.0%
Market quality

44 / 100

Low quality
24h Volume

$9.1

Liquidity

$1.8K

Low liquidity
Bid / Ask

76.0% / 79.0%

Spread

4.0%

Moderate spread
Market data

Updated 2 minutes ago

Jun 4, 26, 8:04 PMJun 29, 26, 12:00 AM

Trends

Outcome24hChance

Selected outcome

Yes78%

Rules

As of market creation, the FDA's expected decision date for the specified application is June 29, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Unicycive's Oxylanthanum carbonate as a treatment for hyperphosphatemia in CKD patients on dialysis by July 13, 2026, 11:59 PM ET.
  • Otherwise, this market will resolve to "No."
  • An approval is defined as: For new drugs: FDA issuance of an approval letter for a New Drug Application (NDA) or Biologics License Application (BLA) For already-marketed drugs seeking new indications: FDA approval of a supplemental NDA (sNDA) or supplemental BLA (sBLA) for the specific indication referenced For generic drugs: FDA approval of an Abbreviated New Drug Application (ANDA) For biosimilars: FDA approval of a 351(k) application
  • The following constitute qualifying approvals: Standard approval (traditional approval based on clinical benefit), Accelerated approval (based on surrogate endpoints), Approval with Risk Evaluation and Mitigation Strategy (REMS), Approval with restricted distribution or indication limitations, except compassionate use/expanded access programs

Related Markets

Hantavirus pandemic in 2026?

Hantavirus pandemic in 2026?

$167.7K
Yes: 5%PolymarketPOLYMARKET
New pandemic in 2026?

New pandemic in 2026?

$19.2K
Yes: 10%PolymarketPOLYMARKET
Ebola pandemic in 2026?

Ebola pandemic in 2026?

$10.1K
Yes: 8%PolymarketPOLYMARKET
Manifold Markets

How many movies will gross >$1 billion in 2026?

$1.5K
0-3: 5.7%Manifold MarketsMANIFOLD MARKETS
Manifold Markets

Which disease will be eradicated next in humans?

$533.9
Polio: 26.7%Manifold MarketsMANIFOLD MARKETS
When, where or how will Trump die?

When, where or how will Trump die?

$159.1
2025: 0%Manifold MarketsMANIFOLD MARKETS

Active in these topics

BitcoinBTC$62,957.29+2.90%EthereumETH$1,659.73+2.21%SolanaSOL$65.37+2.33%DogecoinDOGE$0.0851+2.05%XRPXRP$1.12+1.01%BNBBNB$597.01+2.13%

Related News

Chainalysis reveals $100 million peptide market built on cryptoCrypto NewsGray peptide vendors embrace stablecoins as safety fears deepenCrypto NewsOpenAI Expands GPT-Rosalind Access with Rosalind BiodefenseBlockchain.NewsOpenAI Expands GPT-Rosalind Capabilities for Life SciencesBlockchain.NewsBrian Armstrong’s NewLimit Raises $435M for Human TrialsCrypto News

Rules

As of market creation, the FDA's expected decision date for the specified application is June 29, 2026.

Polymarket
  • This market will resolve to "Yes" if the U.S.
  • Food and Drug Administration (FDA) grants full or conditional approval for Unicycive's Oxylanthanum carbonate as a treatment for hyperphosphatemia in CKD patients on dialysis by July 13, 2026, 11:59 PM ET.
  • Otherwise, this market will resolve to "No."
  • An approval is defined as: For new drugs: FDA issuance of an approval letter for a New Drug Application (NDA) or Biologics License Application (BLA) For already-marketed drugs seeking new indications: FDA approval of a supplemental NDA (sNDA) or supplemental BLA (sBLA) for the specific indication referenced For generic drugs: FDA approval of an Abbreviated New Drug Application (ANDA) For biosimilars: FDA approval of a 351(k) application
  • The following constitute qualifying approvals: Standard approval (traditional approval based on clinical benefit), Accelerated approval (based on surrogate endpoints), Approval with Risk Evaluation and Mitigation Strategy (REMS), Approval with restricted distribution or indication limitations, except compassionate use/expanded access programs