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Telomir Pharmaceuticals Announces FDA Clearance of IND for Telomir-Zn in Triple-Negative Breast Cancer

(Positive)

Telomir Pharmaceuticals (NASDAQ:TELO) announced FDA clearance of its IND for Telomir-Zn to treat advanced or metastatic triple-negative breast cancer (TNBC). The clearance enables a first-in-human, multicenter Phase 1/2 study (TELO-001) planned for 1H 2026 with ~76 patients to assess safety, PK/PD, and preliminary antitumor activity.

The study includes dose escalation and expansion, integrated biomarker analyses of epigenetic modulation and telomere biology, and aims to identify potential predictive biomarkers.

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Positive

  • FDA IND clearance enables clinical evaluation
  • Planned enrollment of approximately 76 patients
  • Phase 1/2 start targeted in 1H 2026
  • Integrated biomarker program for target engagement
  • Oral monotherapy administration

Negative

  • First-in-human study — efficacy unproven in patients
  • Small planned sample size limits definitive efficacy signals
  • TNBC is an aggressive indication with historically poor outcomes

News Market Reaction – TELO

-3.45% 20.1x vol
6 alerts
-3.45% Session close to close
+8.4% Peak Tracked
-15.5% Trough Tracked
$49.85M Market Cap
20.1x Rel. Volume

In the Apr 30 session, TELO declined 3.45%, reflecting a moderate negative market reaction. Argus tracked a peak move of +8.4% during that session. Argus tracked a trough of -15.5% from its starting point during tracking. Our momentum scanner triggered 6 alerts that day, indicating moderate trading interest and price volatility. Trading volume was exceptionally heavy at 20.1x the daily average, suggesting significant selling pressure.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement marks FDA clearance of the IND for Telomir‑Zn in advanced or metastatic triple‑neg...
Analysis

This announcement marks FDA clearance of the IND for Telomir‑Zn in advanced or metastatic triple‑negative breast cancer and outlines a first‑in‑human Phase 1/2 trial targeting 76 patients. It extends a series of Telomir‑Zn milestones, from preclinical efficacy to IND submission and a rights‑consolidating acquisition. Investors may focus on execution of the trial design, emerging safety and activity signals, and the company’s ability to support development given its pre‑revenue status and modest $99.7M market value.

Key Figures

Planned enrollment: 76 patients Annual breast cancer cases: 2.3 million TNBC share of cases: 10–15% +1 more
4 metrics
Planned enrollment 76 patients Planned Phase 1/2 TNBC trial (TELO-001)
Annual breast cancer cases 2.3 million Worldwide new breast cancer diagnoses per year
TNBC share of cases 10–15% Portion of breast cancers classified as triple-negative
Market cap $99,717,487 Pre-news market value of TELO

Historical Context

5 past events · Latest: Apr 24 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Apr 24 Acquisition completion Positive +1.4% Closed TELI acquisition, consolidating global rights to Telomir-Zn.
Mar 31 IND submission Positive +14.0% Submitted IND to FDA for Telomir-Zn in advanced/metastatic TNBC.
Feb 17 Preclinical efficacy data Positive +5.5% Reported broad iron-dependent tumor cell mortality in TNBC models.
Feb 05 Mechanism data Positive -3.5% Showed zinc increase and iron reduction supporting metal-modulation mechanism.
Jan 05 Animal model results Positive +11.2% Demonstrated significant tumor and metastasis reduction in TNBC animal models.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Positive Telomir-Zn milestones have usually coincided with upward price reactions, with one notable selloff on supportive preclinical data.

Recent Company History

Over the last few months, Telomir has advanced Telomir-Zn from preclinical data into regulatory and corporate milestones. On Jan 5, zebrafish TNBC efficacy data preceded a 11.19% move. New mechanistic metal-modulation data on Feb 5 saw shares down 3.45%. Subsequent TNBC cell-line results on Feb 17, IND submission on Mar 31, and the TELI acquisition on Apr 24 led to gains of 5.5%, 14.04%, and 1.45% respectively, setting the stage for today’s IND clearance.

Key Terms

investigational new drug, phase 1/2, triple-negative breast cancer, objective response rate, +4 more
8 terms
investigational new drug regulatory
"FDA has cleared the Company's Investigational New Drug (IND) application"
An investigational new drug is a medication that is still being tested in clinical trials to determine if it is safe and effective for treating a specific condition. For investors, it represents a potential breakthrough that could lead to a new treatment and significant financial gains if successful, but also carries risks since it has not yet been approved for widespread use.
phase 1/2 medical
"Company Plans to Initiate First-in-Human Phase 1/2 Trial in 1H 2026"
Phase 1/2 is a combined early-stage clinical trial that first tests a new drug or treatment for safety and the right dose, then quickly expands to check if it shows any signs of working in patients. For investors, results from a Phase 1/2 study offer an early read on both risk and potential reward—like a prototype test that both confirms a product won’t harm users and suggests whether it could sell—helping guide valuation and development decisions.
triple-negative breast cancer medical
"for the treatment of patients with advanced or metastatic triple-negative breast cancer"
Triple-negative breast cancer is a type of breast cancer that lacks three common markers used to identify and treat the disease effectively. Because it doesn’t respond to some targeted therapies, it can be more difficult to treat and may have a more aggressive progression. This impacts the development of new treatments and can influence the outlook for healthcare companies involved in cancer research and pharmaceuticals.
objective response rate medical
"Primary endpoint is objective response rate (ORR)"
The objective response rate (ORR) is the percentage of patients in a clinical trial whose tumors measurably shrink or disappear according to preset rules. Investors use it as a quick, objective signal of a drug’s ability to produce a clear treatment effect—like counting how many plants visibly respond after applying a new fertilizer—and higher ORR can improve odds of regulatory approval, commercial success, and company valuation.
progression-free survival medical
"Secondary endpoints include duration of response (DoR), progression-free survival (PFS)"
Progression-free survival is the length of time during and after a treatment that a patient's disease does not get worse, measured from the start of treatment until the disease shows measurable signs of progression or the patient dies. Investors care because longer progression-free survival in clinical trials often signals that a drug is effective, improving chances of regulatory approval, market adoption, and revenue potential—think of it as a stopwatch showing how long a therapy can keep the illness at bay.
overall survival medical
"Secondary endpoints include ... overall survival (OS), and safety"
Overall survival is the average or median length of time patients remain alive after starting a treatment or entering a clinical study, measured regardless of cause of death. Investors care because it is a clear, hard measure of a therapy’s real-world benefit — like timing how long a new battery actually runs — and strong improvements in overall survival can drive regulatory approval, market adoption and revenue potential.
pharmacokinetics medical
"designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics"
Pharmacokinetics is the study of how a substance, such as a drug or chemical, moves through and is processed by the body over time. It tracks how it is absorbed, distributed, broken down, and eventually eliminated. For investors, understanding pharmacokinetics helps gauge the effectiveness, safety, and potential risks of new medications or treatments, which can influence a company’s success and valuation in the healthcare industry.
epigenetic medical
"targeting epigenetic and metabolic drivers of cancer and age-related disease"
Epigenetic describes changes that alter how genes are turned on or off without changing the underlying DNA sequence, similar to flipping light switches or adjusting software settings that control a machine. For investors, epigenetic mechanisms matter because they create new targets for drugs, diagnostics, and therapies that can modify disease processes or patient responses, potentially leading to novel products, market opportunities, and long-term revenue streams.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Company Plans to Initiate First-in-Human Phase 1/2 Trial in 1H 2026, Anchored by a Leading U.S. Academic Medical Center.

MIAMI, FL / ACCESS Newswire / April 30, 2026 / Telomir Pharmaceuticals, Inc. (NASDAQ:TELO) ("Telomir" or the "Company"), a clinical-stage biotechnology company developing small-molecule therapeutics targeting epigenetic and metabolic drivers of cancer and age-related disease, today announced that the U.S. Food and Drug Administration (FDA) has cleared the Company's Investigational New Drug (IND) application for its lead candidate, Telomir-Zn, for the treatment of patients with advanced or metastatic triple-negative breast cancer (TNBC).

This IND clearance enables the Company to advance Telomir-Zn into clinical evaluation, representing an important step toward addressing a significant unmet need in patients with advanced or metastatic triple-negative breast cancer, where treatment options remain limited, and outcomes are poor.

IND Clearance and Development Package

The FDA's clearance reflects review of a comprehensive IND submission supporting advancement of Telomir-Zn into clinical evaluation. The submission included pharmacology, toxicology, manufacturing data, and the Company's first-in-human Phase 1/2 clinical study protocol (TELO-001).

The IND package was supported by completed IND-enabling studies, including pharmacology and toxicology evaluations, pharmacokinetic data demonstrating systemic exposure, and preclinical data indicating activity in models of triple-negative breast cancer.

Planned Phase 1/2 Clinical Trial

The planned clinical study (TELO-001) is designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of Telomir-Zn as an oral monotherapy in patients with advanced or metastatic TNBC.

Study Overview

  • First-in-human, multicenter, open-label Phase 1/2 trial

  • Adult patients with advanced or metastatic TNBC who have received prior systemic therapy

  • Planned enrollment of approximately 76 patients

Phase 1: Dose Escalation

  • Modified 3+3 dose-escalation design

  • Evaluation of safety, tolerability, and dose-limiting toxicities

  • Determination of maximum tolerated dose and recommended Phase 2 dose

  • Assessment of pharmacokinetics, pharmacodynamics, and preliminary antitumor activity

  • Integrated biomarker analyses to evaluate epigenetic modulation, gene re-expression, and telomere-related biology associated with cellular aging and genomic stability

Phase 2: Dose Expansion

  • Simon's two-stage design to assess preliminary efficacy

  • Primary endpoint is objective response rate (ORR)

  • Secondary endpoints include duration of response (DoR), progression-free survival (PFS), overall survival (OS), and safety

  • The study will incorporate pharmacokinetic, pharmacodynamic, and biomarker analyses to evaluate target engagement and explore potential correlations between epigenetic modulation and clinical outcomes

Translational and Biomarker Strategy

The study includes an integrated biomarker program designed to evaluate pharmacodynamic activity, target engagement, and potential predictors of response.

Biomarker analyses will assess changes in epigenetic regulation, including global DNA methylation, gene re-expression of epigenetically silenced tumor suppressor pathways, and histone modification patterns associated with tumor biology.

In addition, exploratory analyses will evaluate biomarkers related to cellular aging and genomic stability, including telomere dynamics and associated epigenetic signatures, with the objective of understanding the broader biological activity of Telomir-Zn across oncology and age-related pathways.

The study will also assess correlations between biomarker modulation and clinical outcomes, including preliminary antitumor activity, objective response, and progression-free survival, and may inform identification of potential predictive biomarkers of response.

Clinical Development Strategy

The Company plans to initiate the Phase 1/2 clinical trial in the first half of 2026, anchored by a leading U.S. academic medical center, with potential expansion to additional oncology sites.

Mechanism of Action

Telomir-Zn is an investigational small-molecule designed to represent a novel therapeutic approach and a potentially first-in-class strategy focused on modulation of intracellular metal homeostasis and downstream epigenetic regulation.

Unlike conventional cytotoxic chemotherapy, immune checkpoint inhibition, antibody-drug conjugates, or classic epigenetic drugs, Telomir-Zn is being developed to target metal-dependent epigenetic vulnerabilities that may contribute to tumor progression, treatment resistance, genomic instability, and cancer-associated aging biology.

Preclinical studies indicate that Telomir-Zn alters intracellular iron and zinc balance, modulates iron-dependent chromatin-regulating enzymes, and influences gene expression and cellular pathways associated with tumor biology, genomic stability, and cellular aging.

Clinical Context

Breast cancer is the most commonly diagnosed cancer worldwide, with approximately 2.3 million new cases diagnosed annually, according to the World Health Organization.

Triple-negative breast cancer represents approximately 10 to 15 percent of cases and is associated with aggressive disease biology and limited treatment options, particularly in the advanced or metastatic setting.

Despite available therapies, outcomes remain poor, and TNBC continues to represent a multi-billion-dollar global market with significant unmet medical need.

Management Commentary

"The clearance of our IND, including the Phase 1/2 clinical protocol, marks an important step as we advance Telomir-Zn into clinical evaluation," said Erez Aminov, CEO of Telomir.

"Triple-negative breast cancer remains one of the most difficult cancers to treat in the advanced or metastatic setting, with limited options and consistently poor outcomes. There is a clear need for new therapeutic approaches, and we look forward to evaluating Telomir-Zn in this patient population."

Dr. Itzchak Angel, Chief Scientific Advisor, added:

"Telomir-Zn is designed to target fundamental aspects of tumor biology through modulation of intracellular metal balance and epigenetic regulation. This metal-epigenetic approach represents a differentiated therapeutic strategy that may have relevance not only in triple-negative breast cancer but also across broader cancer and age-related disease biology."

About Telomir Pharmaceuticals

Telomir Pharmaceuticals, Inc. (NASDAQ:TELO) is a clinical-stage biotechnology company developing small-molecule therapeutics targeting epigenetic and metabolic pathways implicated in cancer, aging, and degenerative disease. The Company's lead program, Telomir-1 (Telomir-Zn), is designed to modulate intracellular metal homeostasis and epigenetic regulation.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the Company's plans to initiate clinical trials, clinical development strategy, and the potential therapeutic effects of Telomir-Zn. These statements are based on current expectations and involve risks and uncertainties that could cause actual results to differ materially.

Such risks include, but are not limited to, regulatory developments, the timing and outcome of clinical trials, and the Company's ability to execute its development plans. Additional risks are described in the Company's filings with the U.S. Securities and Exchange Commission, including its Annual Report on Form 10-K. The Company undertakes no obligation to update forward-looking statements except as required by law.

Contact Information

Krystina Quintana
Email: info@telomirpharma.com
Phone: (786) 396-6723

SOURCE: Telomir Pharmaceuticals, Inc



View the original press release on ACCESS Newswire

FAQ

What did Telomir (TELO) announce about Telomir-Zn and FDA IND clearance on April 30, 2026?

The company announced FDA clearance of an IND for Telomir-Zn to treat advanced or metastatic TNBC. According to the company, clearance allows initiation of a first-in-human Phase 1/2 study (TELO-001) to assess safety, PK/PD, and preliminary antitumor activity.

When will Telomir start the TELO-001 Phase 1/2 trial and how many patients are planned?

Telomir plans to start the TELO-001 Phase 1/2 trial in the first half of 2026. According to the company, the study plans approximately 76 patients, including a dose-escalation phase followed by a Simon two-stage dose-expansion assessment.

What are the primary endpoints and design features of the TELO-001 trial (TELO)?

The primary endpoint for Phase 2 is objective response rate (ORR); Phase 1 focuses on safety and dose finding. According to the company, the study uses a modified 3+3 escalation and Simon's two-stage expansion with PK/PD and biomarker analyses.

How does Telomir-Zn work and why is its mechanism notable for TNBC (TELO)?

Telomir-Zn is designed to modulate intracellular metal homeostasis and downstream epigenetic regulation. According to the company, it alters iron and zinc balance to affect chromatin enzymes, gene expression, telomere biology, and pathways linked to genomic stability.

What biomarker analyses will the TELO-001 study include and what will they evaluate?

The study includes integrated biomarker analyses of global DNA methylation, gene re-expression, histone modifications, and telomere dynamics. According to the company, these assays will evaluate target engagement and explore correlations with clinical outcomes.

What does the IND clearance mean for Telomir shareholders and clinical development (TELO)?

IND clearance permits Telomir to begin first-in-human clinical testing of Telomir-Zn, advancing its development program. According to the company, this milestone launches a Phase 1/2 trial that will generate initial human safety, PK/PD, biomarker, and preliminary efficacy data.