The company behind TRE-515

A clinical-stage biotechnology company advancing a first-in-class oral therapy across oncology, autoimmune disease, and ALS, built on more than a decade of UCLA research.

Clinical-Stage

A UCLA spinout, Trethera spent its early years advancing the science before entering the clinic.

Lead Program: TRE-515

A first-in-class oral therapy with potential across oncology, autoimmune disease, and ALS.

>$17 in Non-Dilutive Funding

Secured primarily through NIH grants as of July 2026, without diluting shareholder equity.

The company behind TRE-515

A clinical-stage biotechnology company advancing a first-in-class oral therapy across oncology, autoimmune disease, and ALS, built on more than a decade of UCLA research.

Clinical-Stage

A UCLA spinout, Trethera spent its early years advancing the science before entering the clinic.

Lead Program: TRE-515

A first-in-class oral therapy with potential across oncology, autoimmune disease, and ALS.

>$17 in Non-Dilutive Funding

Secured primarily through NIH grants as of July 2026, without diluting shareholder equity.

Our mission

Give a family their person back.

Our approach starts with precision. Our drug, TRE-515 selectively shuts down the Salvage Pathway, Under conditions of rapid proliferation and stress, some cancer cells and activated immune cells become increasingly reliant on the Salvage Pathway to reproduce. TRE-515 is a first-in-class oral therapy designed to inhibit the Salvage Pathway and thereby degrade the ability of aberrant cells to rapidly reproduce, impacting cancer, autoimmune disease, and ALS. This is why one drug can plausibly reach across oncology, autoimmune disease, and neurological conditions like ALS.

We’re not chasing every disease at once. We’re data-driven, prioritizing which indications to pursue first base on the preclinical and clinical data, because the fastest way to give more families their person back is to stay disciplined about the science.

Patients fight for the people they love. Our work is to give that fight better odds. Because when one person faces a disease, the whole family faces it with them.

Patients fight for the people they love. Our work is to give that fight better odds. Because when one person faces a disease, the whole family faces it with them.

Our mission

Give a family their person back.

Our approach starts with precision. TRE-515 targets the Salvage Pathway directly, which is why one drug can plausibly reach across oncology, autoimmune disease, and neurological conditions like ALS. Every indication we pursue is chosen by following the data, not a hunch.

We’re not chasing every disease at once. We’re following one mechanism wherever the evidence says it works, because the fastest way to give more families their person back is to stay disciplined about the science, not the size of the ambition.

Patients fight for the people they love. Our work is to give that fight better odds. Because when one person faces a disease, the whole family faces it with them.

Leadership

Guided by Scientists and Builders.

Trethera has demonstrated growth through an expansion of potential disease indications, new patents, and exceptional talent.

With FDA Orphan Drug designations for two indications, a Fast Track designation for another, and a clear roadmap to commercialization, Trethera is well-positioned for both patient impact and investor value.

Management

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Advisors

Board of Directors

Our History

From UCLA to present day

Trethera’s path traces a single idea, that blocking the Salvage Pathway could selectively stop the cells driving disease.

2009

T&B cells use dCK

UCLA scientists demonstrate that dCK inhibition affects T & B cell development.

2012

dCK deficiency impacts developing T&B cells

Genetic dCK loss depletes dCTP inducing replication stress and impairing developing T and B lymphocytes.

2014

Scientists synthesize dCK inhibitors

UCLA demonstrates targeting DNP and dCK is effective in leukemia cancer models. Scientists also synthesize dCK inhibitors (incl. TRE-515) with favorable PK properties.

2016

A broadening pipeline

Scientists demonstrate a clinically translatable PET probe to measure intracellular dCK activity.

2017-2020

TRE-515 selected for development

Candidate selection & pharmaceutical development.

2021-2023

Orphan Drug designations and Clinical Trial begins

TRE-515 clinical oncology trial initiated; TRE-515 awarded Orphan Drug designation for optic neuritis and ADEM.

2025

Phase 1 dose escalation complete

The dose escalation portion of the first-in-human trial for advanced solid tumors complete, establishing a therapeutic window and safety profile and opening up the dose expansion phase.

2026

Building momentum

TRE-515 + Radiation receives FDA Fast Track designation in prostate cancer, a new peer-reviewed oncology paper is published, and non-dilutive funding surpasses $17M.

2009

T&B cells use dC

UCLA scientists demonstrate that dCK inhibition affects T & B cell development.

2012

dCK inihibtion damages T&B cekks

Scientists demonstrate dCK inhibition depletes dCTP, induces DNA replication stress and DNA damage in B & T lympphocytes.

2014

Scientists synthesize dCK inhibitors

UCLA demonstrates targeting DNP and dCK is effective in leukemia cancer models. Scientists also synthesize dCK inhibitors (incl. TRE-515) with favorable PK propertires.

2016

A broadening pipeline

Scientists demonstrate a clinically translatable PET probe to measure intracellular dCK activity.

2017-2020

TRE-515 selected for development

Candidate selection & pharmaceutical development.

2021-2023

FDA clearance and Orphan Drug designations

FDA clears TRE-515 oncology IND; designates Orphan Drug for optic neuritis and ADEM.

2025

Phase 1 dose escalation complete

The first-in-human dose-escalation trial for advanced solid tumors complete first-in-human, establishing a therapeutic window and safety profile.

2026

Building momentum

TRE-515 receives FDA Fast Track designation in prostate cancer, a new peer-reviewed oncology paper is published, and non-dilutive funding surpasses $17M.