![](https://investorshub.advfn.com/uicon/401478.png?cb=1525759637)
Wednesday, November 29, 2017 12:28:21 PM
Their treatment is administered systemically and therefore yields a high rate of adverse events. Their phase 1 trial yielded interim results where nearly a 3rd of the 34 participants experienced level III and IV adverse events – – I think that’s pretty high – – I’m also curious about the cost being prohibitive.
I am also very biased regarding the Merck/Keytruda Connection. It’s hard to see Merck, after millions of dollars of drug investment, should the multigene cocktail prove as well as we hope, to then just hand over billions in potential profit derived from Oncosec to the highest bidder. Also, I don’t believe the FDA would allow the free interchange of PD – 1’s as though they are all created equal clinically speaking, and that concerns for safety would mean more safety trials, which is not at all expedient of a process for OncoSec. So I think both companies are stuck with each other and so far I don’t think it’s a bad relationship
![smile](/images/emoticon01.gif)
Recent ONCSQ News
- Form SC 13G/A - Statement of acquisition of beneficial ownership by individuals: [Amend] • Edgar (US Regulatory) • 02/13/2024 07:30:19 PM
Cannabix Technologies and Omega Laboratories Inc. Provide Positive Developments on Marijuana Breathalyzer Testing • BLO • Jul 11, 2024 8:21 AM
ECGI Holdings Enhances Board with Artificial Intelligence (AI) Expert Ahead of Allon Apparel Launch • ECGI • Jul 10, 2024 8:30 AM
Avant Technologies to Meet Unmet Needs in AI Industry While Addressing Sustainability Concerns • AVAI • Jul 10, 2024 8:00 AM
Panther Minerals Inc. Launches Investor Connect AI Chatbot for Enhanced Investor Engagement and Lead Generation • PURR • Jul 9, 2024 9:00 AM
Glidelogic Corp. Becomes TikTok Shop Partner, Opening a New Chapter in E-commerce Services • GDLG • Jul 5, 2024 7:09 AM
Freedom Holdings Corporate Update; Announces Management Has Signed Letter of Intent • FHLD • Jul 3, 2024 9:00 AM