Monday, October 24, 2022 4:13:41 PM
PFS is an fully approvable endpoint by regulators and is commonly used in GBM clinical trials. Even Dr. Liau is using PFS as the lead efficacy endpoint in her Keytruda/DCVax-L combination trial -- did you miss that??
The NWBO OS is confounded by the crossover when patients were all double dosed while comparator was not (internal and external). Regulators are certainly going to question the validity of the OS data because of the confounding.
Recent NWBO News
- Form 8-K - Current report • Edgar (US Regulatory) • 11/01/2024 09:24:13 PM
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- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/09/2024 09:06:07 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 08/08/2024 08:30:09 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/02/2024 02:42:28 PM
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- Form 8-K - Current report • Edgar (US Regulatory) • 06/04/2024 09:11:16 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 06/03/2024 09:22:55 PM
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- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/10/2024 09:04:57 PM
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