公司資料
Ultragenyx Pharmaceutical 股價、新聞與催化劑
- 股票代碼:
- RARE
- 交易所:
- NASDAQ
- 產業:
- Biopharma
- 所在地:
- United States
股票表現
26.13 USD (-1.36%)
收盤價
最後更新: 2026年8月17日
2.15B USD
市值
股價為何變動
As of Aug 17, 2026, RARE closed down 1.36% at $26.13. No new same-company headline was identified in the current news window.
公司概覽
Rare-Disease Portfolio
Ultragenyx Pharmaceutical develops and commercializes therapies for serious rare and ultrarare genetic diseases. Its portfolio spans antisense oligonucleotides, enzyme and small-molecule medicines, and adeno-associated virus gene therapies.
GTX-102 for Angelman Syndrome
GTX-102, or apazunersen, is an antisense oligonucleotide designed to reactivate the normally silenced paternal copy of UBE3A in neurons. It is being evaluated in the Phase 3 Aspire study for patients with a full maternal UBE3A deletion and the Phase 2/3 Aurora study across other genotypes and age groups.
DTX401 for GSDIa
DTX401, or pariglasgene brecaparvovec, is an AAV8 gene therapy under FDA review for glycogen storage disease type Ia. The program is designed to restore glucose-6-phosphatase activity and improve metabolic control through one-time treatment.
UX111 for Sanfilippo Syndrome
UX111, or rebisufligene etisparvovec, is an AAV9 gene therapy under FDA review for Sanfilippo syndrome type A. The resubmitted application seeks accelerated approval in a progressive pediatric neurodegenerative disease.
DTX301 for OTC Deficiency
DTX301, or avalotcagene ontaparvovec, is an AAV8 gene therapy for ornithine transcarbamylase deficiency. The Phase 3 program has demonstrated a reduction in 24-hour plasma ammonia, supporting continued development toward registration.
未來催化劑
- Phase 3 Aspire data for GTX-102 expected in the second half of 2026.
- Completion of enrollment in the Phase 2/3 Aurora study expected in the second half of 2026.
- FDA action on the DTX401 BLA expected by August 23, 2026.
- FDA action on the UX111 BLA expected by September 19, 2026.
- Additional DTX301 clinical data expected in the first half of 2027.
近期新聞
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