Welcome to our dedicated page for Pharmacyte Biotech SEC filings (Ticker: PMCB), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Pharmacyte Biotech’s Cell-in-a-Box capsules may one day localize chemotherapy inside a pancreatic tumor or replace daily insulin injections, but the science that excites clinicians can overwhelm investors. Clinical timelines, R&D spend, and dilution risk hide in pages of dense disclosures. That’s why the most common Google questions—“Where are Pharmacyte Biotech insider trading Form 4 transactions?” and “How do I read a Pharmacyte Biotech quarterly earnings report 10-Q filing?”—keep surfacing.
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PharmaCyte Biotech, Inc. is soliciting votes at a virtual special meeting to consider several proposals including approval of an issuance proposal, an amendment to the 2022 Equity Incentive Plan to add 2,250,000 shares available for awards, and an adjournment proposal to permit additional solicitation if needed. The proxy materials include voting methods (by mail or during the virtual meeting) and a security ownership table showing entities affiliated with Intracoastal Capital LLC hold 714,844 shares (about 10.23%) and all directors and executive officers as a group hold 770,230 shares (about 10.33%), with Chairman/CEO Joshua N. Silverman shown with 220,000 shares (approximately 3.16%). The materials reference the full text of the amended Equity Incentive Plan in an appendix.
PharmaCyte Biotech, Inc. (PMCB) filed an S-3 shelf registration to register shares issuable upon conversion of Series C Preferred Stock and upon exercise of outstanding warrants and placement agent warrants. The prospectus notes the company would receive up to approximately $7.5 million only if all warrants are exercised for cash; otherwise selling stockholders will receive proceeds from secondary sales. The registration covers shares held by multiple institutional and individual selling stockholders (many pegged at 4.99% ownership thresholds) and includes a 150% sizing convention used to calculate maximum conversion and warrant share counts. The document reiterates significant risks including a clinical hold interaction with the FDA on an IND for a planned LAPC clinical trial, long drug-development timelines, dependence on third parties, potential illiquidity, and general regulatory and competitive risks. The offering may enable secondary liquidity but also creates potential dilution if conversions/exercises occur.
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