Shuttle Pharmaceuticals Receives FDA Approval to Proceed with Phase II Clinical Trial of Ropidoxuridine for Treatment of Patients with Glioblastoma [Yahoo! Finance]
Shuttle Pharmaceuticals Holdings, Inc. (SHPH)
Company Research
Source: Yahoo! Finance
Food and Drug Administration (FDA) for the Company's investigational new drug (IND) application for its Phase II study of Ropidoxuridine (IPdR) as a radiation sensitizing agent during radiotherapy in patients with newly diagnosed IDH-wildtype glioblastoma with unmethylated MGMT promoter. Receipt of the letter allows Shuttle to commence the Phase II study. Shuttle Pharma is currently finalizing site enrollment with 'first patient, first dose' expected in the coming months. Ropidoxuridine is Shuttle Pharma's lead radiation sensitizer candidate for use in combination with radiation therapy (RT) to treat glioblastoma, a deadly malignancy of the brain with no known cure. "We are excited to have been granted approval to commence Ropidoxuridine's Phase II clinical trial following the receipt of the FDA's 'Safe to Proceed' letter," stated Shuttle Pharma's Chairman and CEO, Anatoly Dritschilo , M.D. "Radiation therapy is a proven modality for treating cancers. However, there is a significa
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News
- Shuttle Pharmaceuticals to Present at the Planet MicroCap Showcase: VEGAS 2024 on Wednesday, May 1, 2024 & 1x1 Meetings on Thursday, May 2, 2024 [Yahoo! Finance]Yahoo! Finance
- Shuttle Pharmaceuticals to Present at the Planet MicroCap Showcase: VEGAS 2024 on Wednesday, May 1, 2024 & 1x1 Meetings on Thursday, May 2, 2024GlobeNewswire
- Shuttle Pharmaceuticals to Present at the Emerging Growth Conference on April 4, 2024GlobeNewswire
- Shuttle Pharma Provides Fourth Quarter 2023 Corporate Update [Yahoo! Finance]Yahoo! Finance
- Shuttle Pharma Provides Fourth Quarter 2023 Corporate UpdatePR Newswire
SHPH
Sec Filings
- 4/23/24 - Form 8-K
- 4/5/24 - Form S-1
- 3/22/24 - Form 8-K
- SHPH's page on the SEC website