Zevra’s MIPLYFFA™ (arimoclomol) Receives Approval from U.S. Food and Drug Administration for Use in Patients with Niemann-Pick Disease Type C (NPC)
XOMA Royalty Corporation (XOMA)
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Source: GlobeNewswire
MIPLYFFA™ is the first therapy approved for use in patients with NPC, a rare genetic disorder XOMA Royalty is entitled to receive a mid-single digit royalty on MIPLYFFA™ sales and up to $52.6 million in milestones MIPLYFFA™ is now the sixth commercial asset in XOMA Royalty’s portfolio EMERYVILLE, Calif., Sept. 23, 2024 (GLOBE NEWSWIRE) -- XOMA Royalty Corporation (NASDAQ: XOMA), the biotech royalty aggregator, announced today Zevra Therapeutics has received approval from the U.S. Food and Drug Administration (FDA) for MIPLYFFA™ (arimoclomol). MIPLYFFA™ is approved for use in combination with miglustat for the treatment of neurological manifestations of Niemann-Pick disease type C (NPC) in adult and pediatric patients two years of age and older. It is the sixth commercial asset in XOMA Royalty’s growing royalty and milestone portfolio. “With the approval of MIPLYFFA™, NPC patients in the United States now have access to the first FDA approved therapeutic in this rare, progress
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XOMA
News
- XOMA Royalty Declares Quarterly Preferred Stock DividendsGlobeNewswire
- XOMA Co. (NASDAQ: XOMA) had its "buy" rating re-affirmed by analysts at HC Wainwright. They now have a $117.00 price target on the stock.MarketBeat
- XOMA Royalty to Present at Upcoming Investor Conferences in SeptemberGlobeNewswire
- XOMA Co. (NASDAQ: XOMA) had its price target raised by analysts at HC Wainwright from $74.00 to $117.00. They now have a "buy" rating on the stock.MarketBeat
- XOMA Co. (NASDAQ: XOMA) was upgraded by analysts at StockNews.com from a "sell" rating to a "hold" rating.MarketBeat
XOMA
Earnings
- 8/13/24 - Beat
XOMA
Sec Filings
- 9/23/24 - Form 8-K
- 8/13/24 - Form 8-K
- 8/13/24 - Form 10-Q
- XOMA's page on the SEC website