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GTBP Overview

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Intellectia

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High
0.431
Open
0.425
VWAP
0.42
Vol
294.93K
Mkt Cap
13.88M
Low
0.411
Amount
123.92K
EV/EBITDA(TTM)
--
Total Shares
31.55M
EV
7.07M
EV/OCF(TTM)
--
P/S(TTM)
--
GT Biopharma, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on the development and commercialization of immuno-oncology therapeutic products based on its proprietary Tri-specific Killer Engager (TriKE) natural killer (NK) cell engager platform. Its TriKE platform is designed to harness and enhance the cancer-killing abilities of a patient’s immune system’s natural killer cells. Its product candidate pipeline includes GTB-3550, GTB-3650, GTB-5550, GTB-7550, GTB-6550, GTB-1050, and other product candidates. GTB-3550 is a TriKE comprised of two single-chain variable fragments (scFv) composed of the variable regions of the heavy and light chains of anti-CD16 and anti-CD33 antibodies and a modified form of IL-15. GTB-3650 is a TriKE which targets CD33 on the surface of myeloid leukemias. The Company also has a worldwide license agreement with the University of Minnesota to further develop and commercialize therapies using TriKE technology.
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Events Timeline

(ET)
2026-03-02
07:10:00
Company Anticipates Cash Balance of Approximately $9 Million by 2026
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2026-02-03 (ET)
2026-02-03
08:40:00
GT Biopharma Receives FDA Clearance for GTB-5550 IND Application
select
2026-01-15 (ET)
2026-01-15
08:40:00
GT Biopharma Submits IND Application for GTB-5550
select
2025-11-14 (ET)
2025-11-14
09:04:37
GT Biopharma announces Q3 net loss of $3.1M, down from $3.4M the previous year.
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2025-10-23 (ET)
2025-10-23
09:05:35
GT Biopharma announces enrollment progress for GTB-3650 Phase 1 trial
select
2025-10-08 (ET)
2025-10-08
09:08:52
GT Biopharma Shares Enrollment Progress for GTB-3650 Phase 1 Trial
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2025-08-11 (ET)
2025-08-11
07:16:01
GT Biopharma advances into cohort 3 of GTB-3650 Phase 1 trial
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News

seekingalpha
9.5
03-02seekingalpha
GT Biopharma Reports $28.4 Million Net Loss for FY2025
  • Financial Performance: GT Biopharma reported a net loss of approximately $28.4 million for FY2025, significantly increasing from a $13.2 million loss in the previous year, indicating pressure in market competition and challenges in profitability.
  • Operating Loss: The company recorded an operating loss of about $12.4 million for FY2025, an improvement from $14.4 million the prior year, primarily due to significant reductions in R&D expenses, demonstrating efforts in cost control.
  • Cash Position: As of December 31, 2025, GT Biopharma had approximately $7 million in cash and cash equivalents, with an anticipated proforma cash balance of around $9 million by January 31, 2026, which is expected to be sufficient to fund operations through Q4 2026, ensuring short-term financial stability.
  • R&D Spending: While the company reduced R&D expenditures in FY2025, it remains crucial to monitor future funding utilization to ensure ongoing innovation and market competitiveness, particularly in the rapidly evolving biopharmaceutical sector.
Newsfilter
9.0
02-03Newsfilter
GT Biopharma Initiates Phase 1 Trial for GTB-5550
  • FDA Approval for Trial: GT Biopharma has received FDA clearance to proceed with the Phase 1 clinical trial for GTB-5550, expected to start in mid-2026, marking a significant advancement in NK cell therapy that could provide new treatment options for various solid tumor patients.
  • Strong Cash Position: As of January 31, 2026, GT Biopharma anticipates an unaudited proforma cash balance of approximately $9 million, which is expected to extend its cash runway through Q4 2026, ensuring funding for its clinical trial operations.
  • Innovative Trial Design: The Phase 1 trial of GTB-5550 will utilize a dual nanobody TriKE® approach administered via subcutaneous injection, testing up to six dose levels to identify the maximum tolerated dose (MTD), providing a more patient-friendly administration experience.
  • Multiple Cancer Indications: The trial will prioritize enrollment of patients with advanced prostate, ovarian, and pancreatic cancers who have failed standard therapies, aiming to evaluate the safety and preliminary anti-tumor activity of GTB-5550 across various metastatic disease cohorts, which holds significant clinical implications.
Globenewswire
7.5
01-16Globenewswire
Ventripoint Partners with Nisg̱a'a to Enhance Cardiac Diagnostics with AI Technology
  • Cardiac Diagnostic Innovation: Ventripoint Diagnostics partners with Nisg̱a'a Valley Health Authority to deploy AI-driven 3D heart mapping technology, significantly reducing diagnosis times and addressing accessibility issues for patients in remote areas, thereby enhancing the company's competitive edge in the medical technology sector.
  • Portable Technology Application: The company integrates multi-million dollar MRI capabilities into portable ultrasound devices, enabling hospital-grade cardiac diagnostics at primary care facilities, which reduces patient referral needs and improves healthcare service efficiency.
  • Market Demand Response: As the healthcare industry faces increasing demand for visual diagnostics in 2026, Ventripoint's technological solutions not only meet urgent patient needs but also open new market opportunities, strengthening its strategic position in healthcare infrastructure development.
  • Long-Term Growth Potential: By providing efficient cardiac diagnostic tools, Ventripoint is laying the groundwork for future healthcare infrastructure, showcasing its long-term growth potential in the global medical market.
Newsfilter
7.5
01-16Newsfilter
Ventripoint Partners with Nisg̱a'a Valley to Enhance Cardiac Diagnostics
  • Cardiac Diagnostic Innovation: Ventripoint Diagnostics partners with Nisg̱a'a Valley Health Authority to deploy AI-driven 3D heart mapping, eliminating geographic blind spots in cardiac care and enabling rapid access to high-quality diagnostics for patients in remote areas, significantly enhancing healthcare accessibility.
  • Portable Technology Application: The company integrates multi-million dollar MRI capabilities into portable ultrasound devices, allowing hospital-grade diagnostics to be performed at primary care facilities, thereby reducing patient referral needs and improving healthcare efficiency and patient experience.
  • Market Demand Response: As the demand for rapid heart diagnostics increases among patients, Ventripoint's technology not only meets this urgent need but also establishes a benchmark in healthcare infrastructure, potentially attracting more investment and partnership opportunities.
  • Strategic Positioning: By introducing advanced diagnostic technology to primary healthcare, Ventripoint is providing a blueprint for future healthcare infrastructure development, demonstrating its strategic significance in improving public health and driving medical innovation.
PRnewswire
8.5
01-16PRnewswire
GT Biopharma Submits IND for GTB-5550 Targeting $362 Billion Solid Tumor Market
  • Market Transformation: The precision medicine sector is projected to grow from $138 billion in 2026 to over $537 billion by 2035, marking a shift towards modular biologics that creates substantial market opportunities for companies like GT Biopharma.
  • New Drug Application: GT Biopharma submitted an IND for GTB-5550 to the FDA in December 2025, targeting the B7-H3 protein to treat various solid tumors, which is expected to significantly enhance the company's competitiveness in cancer treatment.
  • Clinical Trial Progress: The planned Phase 1 trial for GTB-5550 will evaluate its efficacy across seven distinct metastatic disease cohorts, potentially providing critical clinical data to further advance the company's product pipeline.
  • Dual Program Advancement: GT Biopharma is concurrently advancing its Phase 1 trial of GTB-3650, having successfully treated multiple patients with a favorable safety profile, which is expected to significantly expand its addressable patient population.
NASDAQ.COM
8.5
01-15NASDAQ.COM
GT Biopharma Submits IND for GTB-5550, Aiming for 2026 Clinical Trials
  • IND Submission: GT Biopharma has submitted an IND application to the U.S. FDA for GTB-5550, targeting the B7-H3 protein to treat various solid tumors, potentially introducing a new therapeutic option in the $362 billion cancer market.
  • Trial Design: The planned Phase 1 trial, set to begin in 2026, will include seven metastatic disease cohorts and utilize subcutaneous dosing, which is expected to enhance patient tolerability and convenience while monitoring progression-free survival and overall survival over a 12-month period.
  • Platform Technology Advantage: GTB-5550 is built on the company's TriKE platform, featuring a dual nanobody design that activates NK cells and specifically binds to B7-H3 on tumor cells, potentially offering a more effective treatment approach for patients.
  • Strong Financial Position: As of December 31, 2025, the company reported a preliminary cash balance of approximately $7 million, anticipated to extend its cash runway into the third quarter of 2026, thereby enhancing its R&D capabilities and market competitiveness.
Wall Street analysts forecast GTBP stock price to rise
1 Analyst Rating
Wall Street analysts forecast GTBP stock price to rise
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
8.00
Averages
8.00
High
8.00
Current: 0.000
sliders
Low
8.00
Averages
8.00
High
8.00
Roth Capital
Jonathan Aschoff
Buy
downgrade
$8 -> $3
AI Analysis
2026-03-03
Reason
Roth Capital
Jonathan Aschoff
Price Target
$8 -> $3
AI Analysis
2026-03-03
downgrade
Buy
Reason
Roth Capital analyst Jonathan Aschoff lowered the firm's price target on GT Biopharma to $3 from $8 and keeps a Buy rating on the shares. The firm is citing the company evaluating second-generation TriKE GTB-3650 in a Phase 1 trial in rel/ref CD33 expressing hematologic malignancies, predominantly AML and high-risk MDS, with initial data expected in 3Q26 following completion of cohort 5, the analyst tells investors in a research note.
Roth Capital
Buy
downgrade
$8 -> $3
2026-03-02
Reason
Roth Capital
Price Target
$8 -> $3
2026-03-02
downgrade
Buy
Reason
Roth Capital lowered the firm's price target on GT Biopharma to $3 from $8 and keeps a Buy rating on the shares. As of January, GT Biopharma held pro forma cash of $9M, sufficient to fund operations through 2026, the analyst tells investors in a research note. The company is advancing its pipeline with a Phase 1 trial of second-generation TriKE GTB-3650 in relapsed/refractory CD33-positive hematologic malignancies, with initial data expected in 3Q26, and plans to start a Phase 1 basket trial of GTB-5550 in mid-2026 for B7-H3-expressing solid tumors, while financial models have been adjusted for increased dilution, the firm says.
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Valuation Metrics

The current forward P/E ratio for GT Biopharma Inc (GTBP.O) is -0.87, compared to its 5-year average forward P/E of -3.12. For a more detailed relative valuation and DCF analysis to assess GT Biopharma Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-3.12
Current PE
-0.87
Overvalued PE
0.78
Undervalued PE
-7.01

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
0.00
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
0.00
Undervalued EV/EBITDA
0.00

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
0.00
Current PS
0.00
Overvalued PS
0.00
Undervalued PS
0.00

Financials

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Frequently Asked Questions

What is GT Biopharma Inc (GTBP) stock price today?

The current price of GTBP is 0.418 USD — it has decreased -5

What is GT Biopharma Inc (GTBP)'s business?

GT Biopharma, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on the development and commercialization of immuno-oncology therapeutic products based on its proprietary Tri-specific Killer Engager (TriKE) natural killer (NK) cell engager platform. Its TriKE platform is designed to harness and enhance the cancer-killing abilities of a patient’s immune system’s natural killer cells. Its product candidate pipeline includes GTB-3550, GTB-3650, GTB-5550, GTB-7550, GTB-6550, GTB-1050, and other product candidates. GTB-3550 is a TriKE comprised of two single-chain variable fragments (scFv) composed of the variable regions of the heavy and light chains of anti-CD16 and anti-CD33 antibodies and a modified form of IL-15. GTB-3650 is a TriKE which targets CD33 on the surface of myeloid leukemias. The Company also has a worldwide license agreement with the University of Minnesota to further develop and commercialize therapies using TriKE technology.

What is the price predicton of GTBP Stock?

Wall Street analysts forecast GTBP stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for GTBP is8.00 USD with a low forecast of 8.00 USD and a high forecast of 8.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is GT Biopharma Inc (GTBP)'s revenue for the last quarter?

GT Biopharma Inc revenue for the last quarter amounts to 0.00 USD, decreased

What is GT Biopharma Inc (GTBP)'s earnings per share (EPS) for the last quarter?

GT Biopharma Inc. EPS for the last quarter amounts to -2.23 USD, increased 33.53

How many employees does GT Biopharma Inc (GTBP). have?

GT Biopharma Inc (GTBP) has 1 emplpoyees as of March 12 2026.

What is GT Biopharma Inc (GTBP) market cap?

Today GTBP has the market capitalization of 13.88M USD.