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Re: big bopper1 post# 233962

Wednesday, 01/15/2025 1:06:25 PM

Wednesday, January 15, 2025 1:06:25 PM

Post# of 234158
The Company will be prioritizing oncology in 2025, as we believe this indication holds the potential for the highest value return to the Company in the form of a significant partnership and/or drug approval. As recently announced, CytoDyn has received FDA clearance to initiate a Phase II study of leronlimab in patients with relapsed/refractory micro-satellite stable colorectal cancer (CRC). As noted in our prior release, we recently completed the kickoff meeting with Syneos Health, the CRO for the study, and enrollment efforts are set to begin in January. .............

......The second follow-up study involves the administration of CCL4, a drug that directly causes liver fibrosis in mice. This study will clarify if the observed reversal of liver fibrosis is restricted to the MASH/fat deposition pathway or might occur independently of the etiology of fibrosis (e.g. alcohol, viral hepatitis, etc.). The results from both follow-up studies will become available in January. As a side note, we have been contacted by colleagues at a major academic institution who indicated that, if the liver fibrosis reversal results are confirmed in the follow-up studies, they would be interested in funding a pilot study of leronlimab in the treatment of patients with pulmonary fibrosis at their own center.

Some have postulated that this second follow-up study may bring a very surprising update... maybe before month end????? OMG
$$$CYDY$$$ New collaborator coming?... maybe more!! Standing by for the rest of the story.

Hurry Pigeons... get me some more cheapies and step on it. Times a wasting. You sick birds are falling down on the job.
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