"Remember, if he likes the drug and asks for another trial it will never be approved."
This is the drug's best chance IMO. It already took a LONG time to get these trials done, and DORB doesn't have a lot of resources.
"The fred Hutchinson center supplied 47 percent of the patients. since they use the corn oil they would not be able to do a placebo trial so a new trial would never recruit patients.""
One could almost make an argument then that the corn oil should be the placebo.
What hasn't been mentioned recently, and what I think is the biggest sticking point frankly in the data package, is the huge differential in the myelo's and the non-myelos. That has yet to be even plausibly explained, and adds to the concern that the observed survival data is an artifact.
This is the drug's best chance IMO. It already took a LONG time to get these trials done, and DORB doesn't have a lot of resources.
"The fred Hutchinson center supplied 47 percent of the patients. since they use the corn oil they would not be able to do a placebo trial so a new trial would never recruit patients.""
One could almost make an argument then that the corn oil should be the placebo.
What hasn't been mentioned recently, and what I think is the biggest sticking point frankly in the data package, is the huge differential in the myelo's and the non-myelos. That has yet to be even plausibly explained, and adds to the concern that the observed survival data is an artifact.
Recent SNGX News
- Form 8-K - Current report • Edgar (US Regulatory) • 05/28/2026 09:21:17 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 05/28/2026 09:20:17 PM
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- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 05/08/2026 08:16:15 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 05/08/2026 08:14:13 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 05/08/2026 08:12:12 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 05/08/2026 08:10:14 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/08/2026 08:05:35 PM
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- Form 8-K - Current report • Edgar (US Regulatory) • 04/28/2026 11:30:13 AM
- Soligenix Announces Interim Results from the Phase 3 FLASH2 Trial Evaluating HyBryte™ in Treatment of Cutaneous T-Cell Lymphoma • PR Newswire (US) • 04/28/2026 11:30:00 AM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 04/03/2026 04:15:15 AM
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- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 03/31/2026 08:13:29 PM
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 03/31/2026 08:11:25 PM
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- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 03/31/2026 08:08:14 PM
- Soligenix Announces Recent Accomplishments and Year End 2025 Financial Results • PR Newswire (US) • 03/31/2026 11:30:00 AM
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- Soligenix Receives Orphan Drug Designation from the European Commission for SGX945 for the Treatment of Behçet's Disease • PR Newswire (US) • 03/26/2026 11:30:00 AM
