Nuvectis' NXP800 gains FDA ODD for cancer treatment [Yahoo! Finance]
Nuvectis Pharma, Inc. (NVCT)
Company Research
Source: Yahoo! Finance
domain-containing protein 1a (ARID1a)-deficient ovarian, fallopian tube and primary peritoneal cancers. ODD status is granted by the US regulator for treatments of rare diseases affecting fewer than 200,000 people in the US, and offers development incentives. The designation could lead to seven years of marketing exclusivity in the US for NXP800 if it is approved for these specific cancers. An oral GCN2 activator, NXP800 is also part of an investigator-sponsored trial for cholangiocarcinoma treatment. The FDA previously awarded fast track designation to NXP800 for platinum-resistant ovarian carcinoma and ODD for cholangiocarcinoma. Nuvectis Pharma is also developing NXP900, an inhibitor targeting the SRC family of kinases. NXP900's dual inhibition mechanism offers a comprehensive approach to shutting down the SRC signalling pathway. The asset is currently in a Phase 1a dose escalation study. Nuvectis chairman and CEO Ron Bentsur stated: “We are very pleased to have rec
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News
- Nuvectis Pharma CEO Says Increased Dose Intensity Needed To Drive More Efficacy From Ovarian Cancer Lead Drug [Yahoo! Finance]Yahoo! Finance
- Nuvectis Pharma Reports Encouraging NXP800 Interim Data Supporting Ongoing Enrollment in Phase 1b Study in Patients with Platinum-Resistant ARID1a-Mutated Ovarian Cancer [Yahoo! Finance]Yahoo! Finance
- Nuvectis Pharma Reports Encouraging NXP800 Interim Data Supporting Ongoing Enrollment in Phase 1b Study in Patients with Platinum-Resistant ARID1a-Mutated Ovarian CancerGlobeNewswire
- Nuvectis Pharma GAAP EPS of -$0.24 beats by $0.01 [Seeking Alpha]Seeking Alpha
- Nuvectis Pharma, Inc. Reports Third Quarter 2024 Financial Results and Business HighlightsGlobeNewswire
NVCT
Earnings
- 5/7/24 - Beat
NVCT
Sec Filings
- 11/20/24 - Form 4
- 11/18/24 - Form 4
- 11/8/24 - Form 4
- NVCT's page on the SEC website