Preclinical CNS biotechnology · Austin, Texas

Next-generation neuroplastogens for practical psychiatric medicine.

Telesti Therapeutics is developing preclinical small-molecule programs designed to retain therapeutically relevant neuroplasticity while reducing the perceptual, safety and operational limitations associated with first-generation psychedelic compounds.

Lead program UL-01 · Preclinical lead optimization
The development problem

The biology may be compelling. The product still has to be practical.

Conventional psychedelic mechanisms can introduce perceptual effects, monitoring requirements and development liabilities that complicate broad clinical use. Telesti is evaluating whether differentiated small-molecule design can preserve relevant pharmacology while improving the path to a scalable medicine.

01
Perceptual effects

Acute subjective effects may affect tolerability, blinding, setting and patient selection.

02
Operational burden

Long monitored visits and specialized delivery models can constrain reach and adoption.

03
Development liabilities

Receptor, cardiac, exposure, formulation and manufacturing risk must be separated and resolved.

Our design thesis

A disciplined route from molecule to candidate.

A compelling receptor profile is not enough. Telesti advances compounds through an integrated, exposure-linked framework spanning functional pharmacology, unbound brain exposure, translational activity, cardiovascular and systemic safety, and candidate-specific developability.

The objective is one development candidate and one genuinely distinct backup—not a broad collection of incompletely characterized leads.

01

Technical truth

Is the foundational package reproducible and decision-ready?

02

Pharmacology

Does the series retain the desired profile without an obvious liability?

03

Exposure

Can tolerated dosing achieve relevant unbound CNS exposure?

04

Translation & safety

Is activity separated from impairment and integrated safety risk?

05

Candidate & CMC

Can the molecule become a controlled, scalable clinical product?

Lead corporate program
UL-01Preclinical lead optimizationSmall molecule

Designed for differentiated neuroplasticity.

UL-01 is being evaluated across functional serotonergic pharmacology, neuroplasticity, CNS exposure, translational models, integrated cardiovascular risk and candidate-specific CMC.

Current objective checkpoint

Development-candidate nomination and a distinct backup supported by a candidate-specific regulatory plan.

DiscoveryHit IDLead opt.PreclinicalIND-enabling
Development discipline

Four systems. One candidate decision.

01
Functional pharmacology

Matched systems, reference compounds and explicit control of assay-dependent conclusions.

02
Exposure & translation

Unbound brain exposure and PK/PD—not nominal dose—anchor in-vivo interpretation.

03
Integrated safety

Functional 5-HT2B, ion channels and in-vivo cardiovascular risk are assessed separately and together.

04
Developability

Solid form, formulation, analytical control, process chemistry and material comparability are candidate-specific.

Company

Scientific ambition with decision discipline.

Telesti combines medicinal chemistry, CNS development strategy and stage-gated execution from Austin, Texas.

Uroš Laban

Uroš Laban, PhD

Co-founder & CSO

Medicinal chemistry and scientific strategy.

Graham Pilger

Graham Pilger

Co-founder & CEO

Strategy, financing, partnerships and program execution.

Work with Telesti

Serious science requires serious partners.

Telesti welcomes inquiries from investors, strategic partners, scientific advisors, government stakeholders, CROs and prospective team members.