Dj Gt Biopharma Inc Com, Inst Holders, 3Q 2025 (Gtbp)

NAPLES, FL / ACCESS Newswire / November 19, 2025 / Patients battling aggressive blood cancers face limited treatment options and uncertain outcomes. Scientists have increasingly turned to the body's own defenses, developing therapies that empower natural killer (NK) cells to seek and destroy malignant cells. These next-generation approaches combine precision, potency, and the potential for fewer side effects than conventional treatments.

The global oncology market is projected to nearly double from $139.4 billion in 2025 to $268.3 billion by 2034, expanding at a compound annual growth rate of 7.5%, according to Global Market Insights Inc. This growth reflects both rising cancer prevalence and increasing demand for innovative, targeted therapies.

Within this landscape, GT Biopharma is advancing a proprietary platform designed to harness NK cells against cancer. Its main candidate, GTB 3650, is currently being tested in Phase 1 trials for patients with relapsed or refractory acute myeloid leukemia, and the company is also working on treatments Early clinical progress and multiple upcoming milestones position GTBP as a notable player in the evolving immuno-oncology market.

Advancing a Potent Platform

GTBP's TriKE platform focuses on NK cell engagers designed to activate and expand a patient's own immune cells. Second-generation TriKE molecules, built with camelid nanobody technology, are reported to be 10 to 40 times more potent than first-generation constructs. The lead program, GTB 3650, is undergoing a Phase 1 dose escalation study targeting CD33-positive hematologic malignancies, including AML and high-risk MDS. The FDA cleared t-positive2024, and enrollment began in January 2025.

Clear Progress in Early Cohorts

The trial includes up to seven cohorts, two patients each, with dose levels ranging from 1.25 µg/kg/day to 100 µg/kg/day. As of October 2025, all six patients in Cohorts 1 through 3 had been successfully treated. The Cohort 3 formal safety review revealed no tolerability issues. enabling progression to Cohort 4 at 10 µg/kg/day. Management described this dose as "more reflective of the potential efficacy threshold," citing positive trends in immunologic biomarkers.

Early cohorts also demonstrated increased NK cell activity, supporting the TriKE mechanism of immune activation and expansion. GTB 3650 is administered as a 72-hour continuous infusion in two-week blocks, allowing assessment of safety, pharmacokinetics, pharmacodynamics, NK cell expansion, and early clinical activity.

Pipeline Growth and Financial Health

GTB 5550, GTBP's B7H3-targeting TriKE, is preparing for an IND submission in late December 2025 or January 2026. This dual camelid nanobody design will use subcutaneous dosing, offering a more patient-friendly alternative to continuous infusion. Preclinical studies support activity against breast, lung, ovarian, pancreatic, bladder, prostate, and head and neck cancers.

Additionally, GTB 7550 targets CD19-positive lymphoid malignancies and autoimmune diseases and remains in preclinical development, with manufacturing plans underway for 2026. GTBP is building a pipeline that spans hematologic, solid tumor, and immune-mediated indications.

Financially, the company reported $2.6 million in cash as of Q3 2025, expected to fund operations into early 2026. R&D expenses decreased year-over-year, while SG&A costs remained stable, reflecting disciplined management during clinical advancement.

GT Biopharma, Inc. is developing a unique NK cell engager platform with several projects targeting blood cancers and solid tumors. Early safety results for GTB 3650, along with signs of immune activation, support the promise of second-generation TriKEs. As they continue to increase doses, prepare for a new solid tumor application, and work on more early-stage programs, GTBP provides investors with several upcoming opportunities while gradually establishing a presence in NK cell-based immuno-oncology.

Mark McKelvie

RazorPitch Inc

https://razorpitch.com/

Markrmckelvie@gmail.com

585 301 7700

SOURCE: GT Biopharma, Inc.

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Net loss narrowed to $5.3M for the nine months ended September 30, 2025, driven by lower R&D and legal costs. Ongoing clinical trials and new financings improved working capital, but substantial doubt remains about the ability to continue as a going concern without additional funding.

Original document: GT Biopharma, Inc. [GTBP] SEC 10-Q Quarterly Report — Nov. 14 2025

Phase 1 trial enrollment for GTB-3650 continues, with next update in Q1 2026. Net loss narrowed to $3.1M in Q3 2025 due to lower R&D expenses, and cash is expected to fund operations into Q1 2026.

Original document: GT Biopharma, Inc. [GTBP] SEC 8-K Current Report — Nov. 14 2025