Developer docs
API playgroundTry for free, no card

Search company profiles

Treadwell Therapeutics

Full company profile

uuid0000scc

Namestring
Treadwell Therapeutics
Legal namestring
Treadwell Therapeutics
Websiteurl
treadwelltx.com
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing novel therapeutics for patients with limited treatment options across hematologic malignancies and solid tumors. The company was founded in July 2019 as a spin-out from the University Health Network (UHN) in Toronto, where all of its small molecule and biologic candidates originated at the Campbell Family Institute. Treadwell pursues previously undrugged oncology vulnerabilities — PLK4, TTK/Mps1, and HPK1 — using small molecule inhibitors, biologics, and TCR-based autologous cell therapies. The entity is governed under Hong Kong SAR law and headquartered administratively in Hong Kong for finance and investor relations; R&D operations are centered at a 9,000 sq-ft facility in Toronto, with additional clinical and business development offices in San Francisco, New York, and Boston. The company has 11-50 employees and operates as a private, venture-backed firm.

The pipeline comprises three clinical-stage small molecule inhibitors: CFI-400945 (ocifisertib), a first-in-class PLK4 inhibitor in Phase 1/2 development for relapsed/refractory AML, MDS, and CMML, which has received FDA Fast Track Designation (April 2022) and Orphan Drug Designation (February 2024); CFI-402257, a best-in-class TTK inhibitor for ER+/HER2- breast cancer after CDK4/6 inhibitor failure, with FDA Fast Track Designation granted January 2023; and CFI-402411, a first-in-class HPK1 inhibitor being evaluated in solid tumors as monotherapy and in combination with pembrolizumab. Preclinical programs include autologous TCR transgenic cell therapies built on the proprietary TCRypt platform (acquired via the October 2021 acquisition of TCRyption Inc.) and internally developed biologics targeting novel immuno-oncology antigens. The drug discovery engine is built around proprietary founder-originated screening platforms — genome-wide RNAi screens, cDNA cell surface protein screens, knockout mice phenotypic analysis, and a Human B-cell Mining Platform for antibody discovery — housed at the Toronto R&D hub.

Treadwell is pre-revenue and funds operations through equity financing and prospective future partnerships. It closed a $91 million Series B in November 2021 co-led by Sino Biopharmaceutical and 3W Fund Management, following an earlier $27 million round in January 2020. In December 2023 the company executed a strategic pipeline prioritization, narrowing focus to its lead AML asset CFI-400945 while reducing its workforce by approximately 30% and signaling openness to partners for non-lead programs. Leadership comprises Acting CEO and CMO Roger Sidhu, M.D. (formerly of Roivant Sciences, Cell Design Labs, and Amgen), Executive Chair Shane Burgess, co-founder and CSO Mark R. Bray, PhD, and co-founder Tak Wah Mak, PhD — credited as the co-discoverer of the T-cell receptor. A Scientific Advisory Board formed in February 2024 includes Carl June, Antoni Ribas, Pasi Jänne, Lillian Siu, Patricia LoRusso, and S. Gail Eckhardt.

Short descriptiontext

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing first-in-class small molecule inhibitors (PLK4, TTK, HPK1), biologics, and TCR-based cell therapies for patients with limited treatment options in AML, MDS, and breast cancer.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersNew York, United States
HQ citystring
New York
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices5 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage oncology, small molecule inhibitors, TCR cell therapy, novel cancer targets, immuno-oncology drugs
Industry1 code
1Molecular Tumor Boards & Clinical Interpretation Services
CodeHLAAANADPrimaryYes
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Clinical-stage Oncology Therapeutics
No data
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Drug Development and Commercialization
TypeOne Time License
Description

Pre-revenue clinical-stage biotechnology company developing novel oncology therapeutics. Revenue expected upon regulatory approval and commercialization of pipeline candidates.

treadwelltx.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Technology or R&D, Operations, Infrastructure, Supply Chain, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing small molecule inhibitors (PLK4, TTK, HPK1), TCR-based cell therapies, and biologics for cancers with limited treatment options including AML, MDS, and ER+/HER2- breast cancer. The company operates an integrated drug discovery and development engine at its Toronto-based R&D hub and has three clinical-stage assets: CFI-400945 (ocifisertib), CFI-402257, and CFI-402411.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • FDA Fast Track Designation granted for CFI-400945 in relapsed/refractory AML (April 2022)
+3 more records
Product overview1 text field

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing a diversified pipeline against novel targets for indications with limited treatment options. The company operates across three therapeutic modalities: (1) Small molecule inhibitors including CFI-400945 (PLK4 inhibitor, ocifisertib), CFI-402257 (TTK inhibitor), and CFI-402411 (HPK1 inhibitor); (2) TCR-based cell therapies utilizing the proprietary TCRypt TCR Identification Platform; and (3) Biologic programs including novel immuno-oncology antibodies. The company's drug discovery and development engine is housed at its Toronto-based R&D hub and includes functional genomics screening approaches, cell surface protein screens, knockout mice technology, and the Human B-cell Mining Platform.

Product and service5 records
1CFI-400945 (Ocifisertib)
CategorySmall molecule kinase inhibitor
Description

First-in-class small molecule inhibitor of Polo-like kinase 4 (PLK4) for the treatment of acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), and chronic myelomonocytic leukemia (CMML). Also under investigation for solid tumors. Demonstrated complete remissions as single agent and in combination with azacitidine in relapsed, adverse risk AML including TP53 mutant disease.

2CFI-402257
CategorySmall molecule kinase inhibitor
Description

Best-in-class small molecule inhibitor of Threonine Tyrosine Kinase (TTK/Mps1) targeting the spindle assembly checkpoint. Investigated for the treatment of ER+/HER2- advanced breast cancer after progression on CDK4/6 inhibitors and endocrine therapy, both as monotherapy and in combination with fulvestrant.

3CFI-402411
CategorySmall molecule immuno-oncology inhibitor
Description

First-in-class small molecule inhibitor of Hematopoietic Progenitor Kinase 1 (HPK1), a pleiotropic negative regulator of immune cell activation. HPK1 inhibition activates T cells, B cells and dendritic cells for immuno-oncology applications. Investigated in solid tumors as monotherapy or in combination with pembrolizumab.

4TCR-based cell therapy programs
CategoryCell therapy
Description

Autologous, TCR transgenic T-cell therapies developed through the proprietary TCRypt TCR Identification Platform for solid and hematologic malignancies with unmet need. The TCRypt platform enables identification of TCRs beyond conventional A*02:01 restriction, expanding the addressable patient population.

5Biologic programs
CategoryBiologics
Description

Internally developed biologic programs representing novel immuno-oncology targets, including a novel immune-oncology target identified through knockout mice technology that forms the basis of an advanced undisclosed antibody program. Developed alongside small molecule and cell therapy programs.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-04-06
Description

Licensing agreement for four novel oncology target programs including preclinical biologic and small molecule assets. Programs were initiated and validated by UHN's Campbell Family Institute at Princess Margaret Cancer Centre. Treadwell was spun out from UHN in 2019.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2021-10-15
Description

Acquired novel TCR-based T-cell therapy company and TIO Bioventures portfolio company. Added TCRypt platform for identifying therapeutically relevant TCRs for autologous cell therapies in solid and hematologic malignancies.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight3 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Agios was co-founded by Treadwell's co-founder Dr. Tak Wah Mak and pursues novel mechanism precision oncology and rare disease therapeutics. Most comparable in scientific lineage, multi-asset clinical pipeline orientation and target-discovery-driven development philosophy.

TypeDirect peer
Description

Black Diamond is a clinical-stage precision oncology company developing small molecule therapies against novel, genetically defined targets. Directly comparable as a small clinical-stage biotech pursuing first-in-class mechanisms with a discovery platform-led approach.

TypeDirect peer
Description

Blueprint Medicines is a precision oncology company developing selective kinase inhibitors against novel targets. Comparable in its focus on genomically defined cancer populations with a multi-asset clinical pipeline of targeted small molecules.

TypeDirect peer
Description

Repare is a clinical-stage precision oncology company developing synthetic lethality-based therapies including synthetic lethal small molecules and CCNE1-targeted assets. Directly comparable as a discovery-platform-driven oncology biotech with multiple programs in early clinical development.

TypeDirect peer
Description

Erasca is a clinical-stage precision oncology company focused on RAS/MAPK pathway therapeutics with a multi-modality pipeline of small molecules. Comparable in targeting well-defined oncogenic pathways with clinical assets of similar development stage.

TypeDirect peer
Description

Foghorn is a clinical-stage oncology company developing therapies against novel chromatin biology targets using a proprietary discovery platform. Comparable as a platform-driven oncology biotech with multiple preclinical and clinical assets targeting under-explored biology.

TypeDirect peer
Description

Arcus is a clinical-stage immuno-oncology company developing small molecules and antibodies targeting novel immune checkpoints and the adenosine pathway. Comparable in combining small molecule and biologic modalities across oncology with multiple clinical programs.

TypeDirect peer
Description

Arvinas is a clinical-stage oncology company pioneering targeted protein degradation using PROTAC technology against previously undruggable targets. Comparable in pursuing first-in-class mechanisms against novel oncology targets through a differentiated platform approach.

TypeDirect peer
Description

IDEAYA is a clinical-stage precision oncology company developing synthetic lethality-based therapies including PARG and MAT2A inhibitors. Comparable as a clinical-stage biotech with a discovery engine targeting novel precision oncology mechanisms in hematologic and solid tumors.

TypeBroad incumbent
Description

Schrodinger operates a broader computational drug discovery platform serving multiple therapeutic areas including oncology, with its own clinical pipeline. Comparable in marrying proprietary discovery technology with internal pipeline development, though it serves a wider set of modalities and customers.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature8 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors6 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Treadwell Therapeutics

Clinical-stage Oncology Therapeuticstreadwelltx.com

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing first-in-class small molecule inhibitors (PLK4, TTK, HPK1), biologics, and TCR-based cell therapies for patients with limited treatment options in AML, MDS, and breast cancer.

What Treadwell Therapeutics does

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing novel therapeutics for patients with limited treatment options across hematologic malignancies and solid tumors. The company was founded in July 2019 as a spin-out from the University Health Network (UHN) in Toronto, where all of its small molecule and biologic candidates originated at the Campbell Family Institute. Treadwell pursues previously undrugged oncology vulnerabilities — PLK4, TTK/Mps1, and HPK1 — using small molecule inhibitors, biologics, and TCR-based autologous cell therapies. The entity is governed under Hong Kong SAR law and headquartered administratively in Hong Kong for finance and investor relations; R&D operations are centered at a 9,000 sq-ft facility in Toronto, with additional clinical and business development offices in San Francisco, New York, and Boston. The company has 11-50 employees and operates as a private, venture-backed firm.

The pipeline comprises three clinical-stage small molecule inhibitors: CFI-400945 (ocifisertib), a first-in-class PLK4 inhibitor in Phase 1/2 development for relapsed/refractory AML, MDS, and CMML, which has received FDA Fast Track Designation (April 2022) and Orphan Drug Designation (February 2024); CFI-402257, a best-in-class TTK inhibitor for ER+/HER2- breast cancer after CDK4/6 inhibitor failure, with FDA Fast Track Designation granted January 2023; and CFI-402411, a first-in-class HPK1 inhibitor being evaluated in solid tumors as monotherapy and in combination with pembrolizumab. Preclinical programs include autologous TCR transgenic cell therapies built on the proprietary TCRypt platform (acquired via the October 2021 acquisition of TCRyption Inc.) and internally developed biologics targeting novel immuno-oncology antigens. The drug discovery engine is built around proprietary founder-originated screening platforms — genome-wide RNAi screens, cDNA cell surface protein screens, knockout mice phenotypic analysis, and a Human B-cell Mining Platform for antibody discovery — housed at the Toronto R&D hub.

Treadwell is pre-revenue and funds operations through equity financing and prospective future partnerships. It closed a $91 million Series B in November 2021 co-led by Sino Biopharmaceutical and 3W Fund Management, following an earlier $27 million round in January 2020. In December 2023 the company executed a strategic pipeline prioritization, narrowing focus to its lead AML asset CFI-400945 while reducing its workforce by approximately 30% and signaling openness to partners for non-lead programs. Leadership comprises Acting CEO and CMO Roger Sidhu, M.D. (formerly of Roivant Sciences, Cell Design Labs, and Amgen), Executive Chair Shane Burgess, co-founder and CSO Mark R. Bray, PhD, and co-founder Tak Wah Mak, PhD — credited as the co-discoverer of the T-cell receptor. A Scientific Advisory Board formed in February 2024 includes Carl June, Antoni Ribas, Pasi Jänne, Lillian Siu, Patricia LoRusso, and S. Gail Eckhardt.

Treadwell Therapeutics firmographics

Firmographics
Name
Treadwell Therapeutics
Legal name
Treadwell Therapeutics
Website
https://treadwelltx.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
11–50 employees
Short description
Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing first-in-class small molecule inhibitors (PLK4, TTK, HPK1), biologics, and TCR-based cell therapies for patients with limited treatment options in AML, MDS, and breast cancer.
Ownership category
akta.pro rank

Treadwell Therapeutics industry classification

Industry
Product category
Clinical-stage Oncology Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Molecular Tumor Boards & Clinical Interpretation Services (HLAAANAD)

Keywords

  • Clinical-stage oncology
  • Small molecule inhibitors
  • TCR cell therapy
  • Novel cancer targets
  • Immuno-oncology drugs

Where Treadwell Therapeutics is headquartered

Location

Headquarters

HQ city
New York
HQ country
United States
HQ region
North America

Offices5 records

Markets served

Treadwell Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Operations, Infrastructure, Supply Chain, Marketing or Sales

Revenue model

  1. Drug Development and Commercialization: Pre-revenue clinical-stage biotechnology company developing novel oncology therapeutics. Revenue expected upon regulatory approval and commercialization of pipeline candidates.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels4 records

Treadwell Therapeutics product offering

Product offering

Core offering

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing small molecule inhibitors (PLK4, TTK, HPK1), TCR-based cell therapies, and biologics for cancers with limited treatment options including AML, MDS, and ER+/HER2- breast cancer. The company operates an integrated drug discovery and development engine at its Toronto-based R&D hub and has three clinical-stage assets: CFI-400945 (ocifisertib), CFI-402257, and CFI-402411.

Product overview

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing a diversified pipeline against novel targets for indications with limited treatment options. The company operates across three therapeutic modalities: (1) Small molecule inhibitors including CFI-400945 (PLK4 inhibitor, ocifisertib), CFI-402257 (TTK inhibitor), and CFI-402411 (HPK1 inhibitor); (2) TCR-based cell therapies utilizing the proprietary TCRypt TCR Identification Platform; and (3) Biologic programs including novel immuno-oncology antibodies. The company's drug discovery and development engine is housed at its Toronto-based R&D hub and includes functional genomics screening approaches, cell surface protein screens, knockout mice technology, and the Human B-cell Mining Platform.

Differentiator

Problem solved

Functional benefit

Products and services

  • CFI-400945 (Ocifisertib) First-in-class small molecule inhibitor of Polo-like kinase 4 (PLK4) for the treatment of acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), and chronic myelomonocytic leukemia (CMML). Also under investigation for solid tumors. Demonstrated complete remissions as single agent and in combination with azacitidine in relapsed, adverse risk AML including TP53 mutant disease.
  • CFI-402257 Best-in-class small molecule inhibitor of Threonine Tyrosine Kinase (TTK/Mps1) targeting the spindle assembly checkpoint. Investigated for the treatment of ER+/HER2- advanced breast cancer after progression on CDK4/6 inhibitors and endocrine therapy, both as monotherapy and in combination with fulvestrant.
  • CFI-402411 First-in-class small molecule inhibitor of Hematopoietic Progenitor Kinase 1 (HPK1), a pleiotropic negative regulator of immune cell activation. HPK1 inhibition activates T cells, B cells and dendritic cells for immuno-oncology applications. Investigated in solid tumors as monotherapy or in combination with pembrolizumab.
  • TCR-based cell therapy programs Autologous, TCR transgenic T-cell therapies developed through the proprietary TCRypt TCR Identification Platform for solid and hematologic malignancies with unmet need. The TCRypt platform enables identification of TCRs beyond conventional A*02:01 restriction, expanding the addressable patient population.
  • Biologic programs Internally developed biologic programs representing novel immuno-oncology targets, including a novel immune-oncology target identified through knockout mice technology that forms the basis of an advanced undisclosed antibody program. Developed alongside small molecule and cell therapy programs.

Quantifiable outcome

  • FDA Fast Track Designation granted for CFI-400945 in relapsed/refractory AML (April 2022)
  • +3 more outcomes

Companies that use Treadwell Therapeutics

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles3 records

Treadwell Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature8 records

Treadwell Therapeutics partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core and major.

  • University Health Network (UHN)coreStrategic or Co-development Partner · 6 April 2022Licensing agreement for four novel oncology target programs including preclinical biologic and small molecule assets. Programs were initiated and validated by UHN's Campbell Family Institute at Princess Margaret Cancer Centre. Treadwell was spun out from UHN in 2019.
  • TCRyption Inc.majorStrategic or Co-development Partner · 15 October 2021Acquired novel TCR-based T-cell therapy company and TIO Bioventures portfolio company. Added TCRypt platform for identifying therapeutically relevant TCRs for autologous cell therapies in solid and hematologic malignancies.

Scale indicators4 records

Recent moves7 records

Expansion highlights3 records

Treadwell Therapeutics competitors and assessment

Company assessment

Direct peers

  • Agios Pharmaceuticals: Agios was co-founded by Treadwell's co-founder Dr. Tak Wah Mak and pursues novel mechanism precision oncology and rare disease therapeutics. Most comparable in scientific lineage, multi-asset clinical pipeline orientation and target-discovery-driven development philosophy.
  • Black Diamond Therapeutics: Black Diamond is a clinical-stage precision oncology company developing small molecule therapies against novel, genetically defined targets. Directly comparable as a small clinical-stage biotech pursuing first-in-class mechanisms with a discovery platform-led approach.
  • Blueprint Medicines: Blueprint Medicines is a precision oncology company developing selective kinase inhibitors against novel targets. Comparable in its focus on genomically defined cancer populations with a multi-asset clinical pipeline of targeted small molecules.
  • Repare Therapeutics: Repare is a clinical-stage precision oncology company developing synthetic lethality-based therapies including synthetic lethal small molecules and CCNE1-targeted assets. Directly comparable as a discovery-platform-driven oncology biotech with multiple programs in early clinical development.
  • Erasca: Erasca is a clinical-stage precision oncology company focused on RAS/MAPK pathway therapeutics with a multi-modality pipeline of small molecules. Comparable in targeting well-defined oncogenic pathways with clinical assets of similar development stage.
  • Foghorn Therapeutics: Foghorn is a clinical-stage oncology company developing therapies against novel chromatin biology targets using a proprietary discovery platform. Comparable as a platform-driven oncology biotech with multiple preclinical and clinical assets targeting under-explored biology.
  • Arcus Biosciences: Arcus is a clinical-stage immuno-oncology company developing small molecules and antibodies targeting novel immune checkpoints and the adenosine pathway. Comparable in combining small molecule and biologic modalities across oncology with multiple clinical programs.
  • Arvinas: Arvinas is a clinical-stage oncology company pioneering targeted protein degradation using PROTAC technology against previously undruggable targets. Comparable in pursuing first-in-class mechanisms against novel oncology targets through a differentiated platform approach.
  • IDEAYA Biosciences: IDEAYA is a clinical-stage precision oncology company developing synthetic lethality-based therapies including PARG and MAT2A inhibitors. Comparable as a clinical-stage biotech with a discovery engine targeting novel precision oncology mechanisms in hematologic and solid tumors.

Broad incumbents

  • Schrodinger: Schrodinger operates a broader computational drug discovery platform serving multiple therapeutic areas including oncology, with its own clinical pipeline. Comparable in marrying proprietary discovery technology with internal pipeline development, though it serves a wider set of modalities and customers.

Market position

Strengths5 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights7 records

Customer concentration

Treadwell Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Treadwell Therapeutics leadership team

Management profile

Number of profiles

Profiles7 records

Treadwell Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Treadwell Therapeutics funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors6 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Treadwell Therapeutics M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Treadwell Therapeutics

What does Treadwell Therapeutics do?

Treadwell Therapeutics is a clinical-stage, multi-modality oncology company developing small molecule inhibitors (PLK4, TTK, HPK1), TCR-based cell therapies, and biologics for cancers with limited treatment options including AML, MDS, and ER+/HER2- breast cancer. The company operates an integrated drug discovery and development engine at its Toronto-based R&D hub and has three clinical-stage assets: CFI-400945 (ocifisertib), CFI-402257, and CFI-402411.

Is Treadwell Therapeutics a public or private company?

Treadwell Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Treadwell Therapeutics founded?

Treadwell Therapeutics was founded in 2019. It employs 11 to 50 people.

Where is Treadwell Therapeutics based?

Treadwell Therapeutics is headquartered in New York, United States, in the North America region.

How does Treadwell Therapeutics make money?

One revenue line is on record: drug Development and Commercialization.

Who are Treadwell Therapeutics's main competitors?

Direct peers on record are Agios Pharmaceuticals, Black Diamond Therapeutics, Blueprint Medicines, Repare Therapeutics, Erasca, Foghorn Therapeutics, Arcus Biosciences, Arvinas and IDEAYA Biosciences. Schrodinger is listed as a broad incumbent.

Does Treadwell Therapeutics have an API?

No public API is recorded for Treadwell Therapeutics.

What industry is Treadwell Therapeutics in?

Treadwell Therapeutics's product category is Clinical-stage Oncology Therapeutics. Its primary akta.pro industry code is HLAAANAD, Molecular Tumor Boards & Clinical Interpretation Services. Its NAICS code is 541714 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
GlobeNewswireTreadwell Therapeutics Announces a Presentation at the 2023 ASH Annual Meeting and Advisory Board MeetingTreadwell Therapeutics announced a presentation of its PLK4 inhibitor CFI-400945 at the 2023 ASH meeting, with a clinical advisory board meeting held on December 10. The drug showed complete remissions in relapsed/refractory AML, including TP53 mutant disease, and dose expansions are planned for 2024 with pivotal studies in 2025.GlobeNewswireTreadwell Announces Strategic Pipeline Prioritization and Leadership TransitionsTreadwell Therapeutics announced it will focus on its PLK4 inhibitor CFI-400945 in relapsed/refractory AML, aiming for a pivotal study in 2025. The company will cut its workforce by approximately 30% and appoint Roger Sidhu as Acting CEO, replacing Shane Burgess and Michael Tusche. It will also explore collaborations for its TTK and HPK1 inhibitors.PR NewswireTreadwell Therapeutics Announces Fast Track Designation Granted by the FDA to CFI-402257 for the Treatment of ER+/HER2- Breast CancerTreadwell Therapeutics announced that the U.S. Food and Drug Administration has granted Fast Track Designation to CFI-402257, a TTK/Mps1 inhibitor, for the treatment of adult patients with ER+/HER2- advanced breast cancer after progression on CDK4/6 inhibitors and endocrine therapy. The designation applies to both monotherapy and combination treatment with fulvestrant. Fast Track status is intended to accelerate development and review of the drug candidate, which has shown early signs of durable activity with a manageable safety profile in this patient population.PR NewswireTreadwell Therapeutics Announces A Presentation at the 2022 ASH Annual Meeting Featuring a Clinical Trial Update on CFI-400945, an oral PLK4 inhibitorTreadwell Therapeutics announced preliminary results from its Phase 2 TWT-202 clinical trial of CFI-400945, an oral first-in-class PLK4 inhibitor, presented at the 2022 ASH Annual Meeting. The trial in 12 patients across three dose cohorts (32, 48, and 64 mg) demonstrated a tolerable safety profile with no dose-limiting toxicities observed and five cases of stable disease. The company indicated plans to continue dose optimization and expand into patient populations with TP53 mutations, where unmet medical need exists.PR NewswireTreadwell Therapeutics Announces A Presentation at the 2022 SABCS Annual Meeting Featuring a Clinical Trial Update on CFI-402257, a Best-in-Class TTK inhibitorTreadwell Therapeutics presented clinical trial data for its CFI-402257 TTK inhibitor at the 2022 San Antonio Breast Cancer Symposium, showing tolerable safety profile and clinical benefit in heavily pre-treated advanced solid tumor patients. The monotherapy achieved a 6% overall response rate (4/66) while combination therapy with fulvestrant in ER+/HER2- breast cancer patients achieved 10% response rate (2/20), with several CDK4/6 inhibitor-failed patients remaining on therapy for over a year. The company indicated plans to further develop the molecule for ER+ breast cancer treatment.PR NewswireTreadwell Therapeutics Announces Presentations at the 2022 San Antonio Breast Cancer Symposium Featuring a Clinical Trial Update on the CFI-402257 and CFI-400945 programsTreadwell Therapeutics announced that four abstracts related to its cancer drug candidates CFI-402257 and CFI-400945 have been accepted for presentation at the 2022 San Antonio Breast Cancer Symposium from December 6-10, 2022. The presentations cover Phase 1 and Phase 2 clinical trials evaluating these TTK and PLK4 inhibitors in patients with HER2-negative breast cancer and triple-negative breast cancer. The trials include both single-agent studies and combination regimens with paclitaxel or durvalumab.PR NewswireTreadwell Therapeutics Announces A Presentation at the 2022 SITC Annual Meeting Featuring a Clinical Trial Update on CFI-402411, a First-in-Class HPK1 inhibitorTreadwell Therapeutics presented interim clinical trial data for CFI-402411, a first-in-class HPK1 inhibitor, at the 2022 SITC Annual Meeting, reporting a clinically manageable safety profile at doses up to 560 mg daily. Among 31 evaluable patients with advanced solid tumors, two patients with head and neck squamous cell carcinoma who had previously failed anti-PD1 therapy achieved partial responses, including one on monotherapy and one on combination therapy with pembrolizumab. The company stated it aims to define the Recommended Phase 2 dose and advance development both as monotherapy and in combination with checkpoint blockade.PR NewswireTreadwell Therapeutics Announces A Presentation at the 2022 SITC Annual Meeting Featuring a Clinical Trial Update on CFI-402411, a First-in-Class HPK1 inhibitorTreadwell Therapeutics announced interim clinical trial results for CFI-402411, a first-in-class HPK1 inhibitor, at the 2022 SITC Annual Meeting in Boston. The Phase 1/2 TWT-101 study showed a manageable safety profile at doses up to 560 mg daily, with 2 partial responses observed among 31 evaluable patients—both in head and neck squamous cell carcinoma patients previously treated with pembrolizumab. The company plans to define the Recommended Phase 2 dose and advance development both as monotherapy and in combination with checkpoint blockade.PR NewswireTreadwell Therapeutics Announces Fast Track Designation Granted by the FDA to CFI-400945 for the Treatment of Acute Myeloid LeukemiaThe FDA granted Fast Track Designation to CFI-400945, a first-in-class PLK4 inhibitor developed by Treadwell Therapeutics, for treating adult patients with relapsed or refractory Acute Myeloid Leukemia. The drug has shown encouraging monotherapy activity in AML patients with adverse cytogenetics, a segment where survival rates remain critically low at approximately 4% for adults over 65. Fast Track designation allows for more frequent FDA interactions and potential pathways for expedited approval.PR NewswireTreadwell Therapeutics Announces A Presentation at the 2021 SABCS Annual Meeting Featuring a Clinical Trial Update on CFI-402257, a Best-in-Class TTK inhibitorTreadwell Therapeutics presented clinical trial data for CFI-402257, its best-in-class TTK inhibitor, at the 2021 San Antonio Breast Cancer Symposium, reporting disease control in 53.2% of heavily pre-treated patients (25 of 67) and 5 confirmed partial responses (10.6%), with 168mg established as the recommended Phase 2 dose. The company plans to initiate a company-sponsored TWT-203 trial in ER+/Her2- breast cancer based on these encouraging results. The presentation (Poster P1-18-17) detailed dose escalation and expansion data from the CFI-402257-CL-001 study in advanced solid tumors.