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Context Therapeutics

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uuid00008i1

Namestring
Context Therapeutics
Legal namestring
Context Therapeutics Inc.
Company typeenum
Public
Founded yearint
2015
Descriptiontext

Context Therapeutics Inc. (NASDAQ: CNTX) is a clinical-stage biopharmaceutical company headquartered in Philadelphia, Pennsylvania, founded in 2015. The company develops T cell engaging (TCE) bispecific antibodies for solid tumors and currently operates with a lean team of 1-10 employees. Context has shifted its strategic focus from its original women's oncology asset (onapristone extended release / ONA-XR) to a portfolio of three next-generation bispecific antibody candidates: CTIM-76 (CLDN6 x CD3), CT-95 (MSLN x CD3), and CT-202 (Nectin-4 x CD3). All three candidates use an IgG format with silenced Fc domains and are engineered to be functionally monovalent to avoid aberrant T-cell activation; CT-202 additionally incorporates BioAtla's pH-dependent Conditionally Active Biologic (CAB) technology for tumor microenvironment selectivity. CTIM-76 was developed using Integral Molecular's MPS antibody discovery platform to isolate rare, highly selective CLDN6 antibodies that avoid cross-reactivity with other CLDN family members.

The pipeline targets multiple solid tumor indications including platinum-resistant ovarian cancer, endometrial, testicular, pancreatic, non-small cell lung, colorectal, triple-negative breast, mesothelioma, and urothelial cancers. CTIM-76 received FDA Fast Track Designation for platinum-resistant ovarian cancer in April 2026, and interim Phase 1 data released in June 2026 showed a 29% confirmed overall response rate and 57% disease control rate in heavily pretreated patients (median 7 prior lines of therapy), with cytokine release syndrome limited to Grade 1 in 11% of patients. All product candidates remain investigational; patient access is provided exclusively through enrollment in company-sponsored Phase 1 clinical trials (NCT06515613, NCT06756035, NCT07545122) and investigator-sponsored trials.

Context's business model is pre-revenue and oriented toward future licensing/royalty income. The company is funded through capital markets, most recently a $100 million private placement completed in May 2024 (lead investor Nextech1, with Ally Bridge Group, Blackstone, Avidity Partners, Blue Owl, Deep Track Capital, Driehaus Capital Management, and Great Point Partners participating). Cash and cash equivalents stood at $66.0 million as of December 31, 2025 (down from $94.4 million at year-end 2024), with management stating the runway extends into mid-2027. The company reported a 2025 net loss of $36.1 million on R&D expenses of $31.9 million, reflecting ramped clinical activity. A legacy exclusive license with Tyligand Bioscience grants Tyligand rights to ONA-XR in China, Hong Kong, and Macau, with Context eligible for royalties on net sales. Market capitalization was approximately $217.75 million as of April 2026, with a consensus 12-month price target of $6.60 from nine research firms.

Short descriptiontext

Context Therapeutics is a clinical-stage biopharmaceutical company developing T cell engaging bispecific antibodies (CTIM-76, CT-95, CT-202) targeting solid tumors including ovarian, pancreatic, lung, breast, and urothelial cancers.

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

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bispecific antibody therapeutics, T cell engager oncology, solid tumor immunotherapy, clinical stage biopharmaceutical, targeted cancer therapy
Industry2 codes
PRIMARYHLAAAAAF
Bispecific & Multispecific Antibodies
Healthcare & Life Sciences/Biotechnology & Biologics/Therapeutic Biologics (mAbs, recombinant proteins, cytokines)
SECONDARYHLAAAIAB
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
Healthcare & Life Sciences/Biotechnology & Biologics/Biologic Drug Discovery Platforms (screening, antibody engineering, synthetic biology)
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Oncology Biopharmaceuticals
Social media profiles2 records
Revenue model1 record
1No Commercial Revenue
TypeLicensing Royalties
Description

Context Therapeutics is a clinical-stage biopharmaceutical company with no commercialized products and no current revenue. All product candidates are investigational and have not received regulatory approval. Revenue will depend on successful development and commercialization of its bispecific antibody pipeline.

biospace.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1CTIM-76
Description

CLDN6 x CD3 bispecific antibody for solid tumors

contexttherapeutics.com
+2 more records
Core offering1 text field

Context Therapeutics develops T cell engaging (TCE) bispecific antibody therapies that bridge tumor cells with T cells to drive immune-mediated killing of solid tumor cancers. Its clinical pipeline comprises three investigational candidates: CTIM-76 (Claudin 6 x CD3), CT-95 (Mesothelin x CD3), and CT-202 (Nectin-4 x CD3), all engineered in an IgG format with silenced Fc for functional monovalency and improved safety. All product candidates are investigational and not yet commercially available.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 29% confirmed overall response rate in heavily pretreated platinum-resistant ovarian cancer patients (median 7 prior lines of therapy) with 57% disease control rate
+4 more records
Product overview1 text field

Context Therapeutics is a clinical-stage biopharmaceutical company advancing T cell engaging (TCE) bispecific antibody therapies for solid tumors. The company's pipeline consists of three clinical-stage bispecific antibody product candidates: CTIM-76 (Claudin 6 x CD3), CT-95 (Mesothelin x CD3), and CT-202 (Nectin-4 x CD3). These TCEs are engineered antibodies designed to bridge tumor cells with T cells to activate immune-mediated cancer cell killing.

Product and service3 records
1CTIM-76
CategoryOncology Biopharmaceutical - Bispecific Antibody
Description

CTIM-76 is an investigational Claudin 6 (CLDN6) x CD3 bispecific T cell engaging antibody being developed for solid tumors including ovarian, endometrial, testicular, and gastric cancers. It incorporates a highly selective CLDN6 binding arm developed using Integral Molecular's MPS antibody discovery platform, paired with a CD3 binding scFv domain in an IgG format with silenced Fc to drive T cell-mediated tumor cell killing.

2CT-95
CategoryOncology Biopharmaceutical - Bispecific Antibody
Description

CT-95 is an investigational mesothelin (MSLN) x CD3 bispecific T cell engaging antibody being developed for MSLN-positive solid tumors including mesothelioma, ovarian cancer, pancreatic adenocarcinoma, non-small cell lung cancer, and triple-negative breast cancer. It features moderate-affinity MSLN binding arms designed to overcome shed mesothelin through membrane-proximal antigen binding.

3CT-202
CategoryOncology Biopharmaceutical - Bispecific Antibody
Description

CT-202 is an investigational Nectin-4 x CD3 bispecific T cell engaging antibody being developed for Nectin-4-positive solid tumors including bladder, non-small cell lung, colorectal, breast, and head and neck cancers. It incorporates BioAtla's Conditionally Active Biologic (CAB) pH-dependent binding technology that drives activity to the tumor microenvironment while minimizing binding to healthy tissues.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-08-25
Description

Context Therapeutics and Tyligand Bioscience entered into a license agreement in August 2021, granting Tyligand exclusive rights and sole responsibility for development and commercialization of ONA-XR in China, Hong Kong, and Macau. Context retains rest of world rights and is eligible to receive royalties on net sales. Tyligand had previously completed ONA-XR manufacturing process optimization in collaboration with Context.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2021-05-12
Description

Jefferson Health and Context Therapeutics collaborated on a Phase 2 clinical trial of ONA-XR in advanced endometrial cancer, with Jefferson Health dosing the first patient. Context has since shifted strategic focus to T cell engaging bispecific antibodies (CTIM-76, CT-95, CT-202).

Strategic tierCoreTypeTechnology or Integration
Description

Context Therapeutics utilized Integral Molecular's MPS (Membrane Protein Scaffold) antibody discovery platform to isolate and optimize rare antibodies against CLDN6 that do not cross-react with other CLDN family members. This platform technology was critical to the development of CTIM-76's highly selective CLDN6 binding arm.

Strategic tierCoreTypeTechnology or Integration
Description

CT-202 incorporates BioAtla's Conditionally Active Biologic (CAB) technology that uses pH dependency to drive localized antibody activity to the tumor microenvironment, minimizing binding to healthy tissues.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage immuno-oncology company developing T cell engager (TCE) bispecific antibodies for solid tumors using its proprietary TRACTr platform. Janux is one of the closest publicly traded pure-play peers to Context's TCE bispecific strategy.

TypeDirect peer
Description

Developed T cell engaging trispecific and bispecific antibodies for solid tumors (e.g., HPN328, HPN217) using its TriTAC and ProTriTAC platforms; acquired by Merck for ~$680M in March 2024. Harpoon is a direct comparable and its former CMO (Luke Walker) is on Context's board.

TypeDirect peer
Description

Developed CONDITIONAL bispecific T cell engagers designed to be activated only in the tumor microenvironment, addressing the same solid-tumor selectivity challenges Context targets with CT-202's CAB technology.

TypeDirect peer
Description

Clinical-stage oncology company developing multiple modalities including TCE bispecifics and immune-engaging antibodies for solid tumors, with a similar profile of small-cap, multi-asset, platform-driven development.

TypeDirect peer
Description

Clinical-stage oncology company developing Probody therapeutics, including masked T cell engaging bispecifics designed to be activated preferentially in the tumor microenvironment — directly analogous to Context's tumor-selective engineering approaches.

TypeDirect peer
Description

Clinical-stage immuno-oncology company developing TCE bispecifics using its POWERbody platform for conditional activation in tumors, with overlapping solid-tumor focus areas (including MSLN).

TypeBroad incumbent
Description

Established biopharmaceutical company and pioneer of the BiTE (bispecific T cell engager) platform, with approved assets Blincyto (CD19 x CD3) and Imdelltra (DLL3 x CD3). Amgen is a broad incumbent with far greater resources and represents the most significant competitive threat in solid-tumor TCEs.

TypeBroad incumbent
Description

Clinical-stage company developing engineered antibody therapeutics including bispecifics via its XmAb platform. Xencor is a broad incumbent in bispecific antibody engineering, with multiple partnered and wholly-owned oncology bispecific programs in solid tumors.

TypeDirect peer
Description

Clinical-stage biopharmaceutical company developing bispecific antibodies for cancer, including DART and TRIDENT platforms. Has multiple solid-tumor bispecific programs and serves as a direct small/mid-cap comparable for Context.

TypeBroad incumbent
Description

Global biopharmaceutical company with a significant oncology franchise and active bispecific antibody development, including TCEs and tumor-targeted immunotherapies. Represents a broad incumbent competitor and potential strategic acquirer of Context's pipeline.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

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 profile2 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

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors9 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&A

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 →

Context Therapeutics

Oncology Biopharmaceuticalscontexttherapeutics.com

Context Therapeutics is a clinical-stage biopharmaceutical company developing T cell engaging bispecific antibodies (CTIM-76, CT-95, CT-202) targeting solid tumors including ovarian, pancreatic, lung, breast, and urothelial cancers.

What Context Therapeutics does

Context Therapeutics Inc. (NASDAQ: CNTX) is a clinical-stage biopharmaceutical company headquartered in Philadelphia, Pennsylvania, founded in 2015. The company develops T cell engaging (TCE) bispecific antibodies for solid tumors and currently operates with a lean team of 1-10 employees. Context has shifted its strategic focus from its original women's oncology asset (onapristone extended release / ONA-XR) to a portfolio of three next-generation bispecific antibody candidates: CTIM-76 (CLDN6 x CD3), CT-95 (MSLN x CD3), and CT-202 (Nectin-4 x CD3). All three candidates use an IgG format with silenced Fc domains and are engineered to be functionally monovalent to avoid aberrant T-cell activation; CT-202 additionally incorporates BioAtla's pH-dependent Conditionally Active Biologic (CAB) technology for tumor microenvironment selectivity. CTIM-76 was developed using Integral Molecular's MPS antibody discovery platform to isolate rare, highly selective CLDN6 antibodies that avoid cross-reactivity with other CLDN family members.

The pipeline targets multiple solid tumor indications including platinum-resistant ovarian cancer, endometrial, testicular, pancreatic, non-small cell lung, colorectal, triple-negative breast, mesothelioma, and urothelial cancers. CTIM-76 received FDA Fast Track Designation for platinum-resistant ovarian cancer in April 2026, and interim Phase 1 data released in June 2026 showed a 29% confirmed overall response rate and 57% disease control rate in heavily pretreated patients (median 7 prior lines of therapy), with cytokine release syndrome limited to Grade 1 in 11% of patients. All product candidates remain investigational; patient access is provided exclusively through enrollment in company-sponsored Phase 1 clinical trials (NCT06515613, NCT06756035, NCT07545122) and investigator-sponsored trials.

Context's business model is pre-revenue and oriented toward future licensing/royalty income. The company is funded through capital markets, most recently a $100 million private placement completed in May 2024 (lead investor Nextech1, with Ally Bridge Group, Blackstone, Avidity Partners, Blue Owl, Deep Track Capital, Driehaus Capital Management, and Great Point Partners participating). Cash and cash equivalents stood at $66.0 million as of December 31, 2025 (down from $94.4 million at year-end 2024), with management stating the runway extends into mid-2027. The company reported a 2025 net loss of $36.1 million on R&D expenses of $31.9 million, reflecting ramped clinical activity. A legacy exclusive license with Tyligand Bioscience grants Tyligand rights to ONA-XR in China, Hong Kong, and Macau, with Context eligible for royalties on net sales. Market capitalization was approximately $217.75 million as of April 2026, with a consensus 12-month price target of $6.60 from nine research firms.

Context Therapeutics firmographics

Firmographics
Name
Context Therapeutics
Legal name
Context Therapeutics Inc.
Website
https://contexttherapeutics.com
Company type
Public
Founded year
2015
Operating status
Operating
Headcount range
11–50 employees
Short description
Context Therapeutics is a clinical-stage biopharmaceutical company developing T cell engaging bispecific antibodies (CTIM-76, CT-95, CT-202) targeting solid tumors including ovarian, pancreatic, lung, breast, and urothelial cancers.
Ownership category
akta.pro rank

Context Therapeutics industry classification

Industry
Product category
Oncology Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834)
akta.pro industry
PRIMARYHLAAAAAF
Bispecific & Multispecific Antibodies
Healthcare & Life Sciences/Biotechnology & Biologics/Therapeutic Biologics (mAbs, recombinant proteins, cytokines)
SECONDARYHLAAAIAB
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
Healthcare & Life Sciences/Biotechnology & Biologics/Biologic Drug Discovery Platforms (screening, antibody engineering, synthetic biology)

Keywords

  • Bispecific antibody therapeutics
  • T cell engager oncology
  • Solid tumor immunotherapy
  • Clinical stage biopharmaceutical
  • Targeted cancer therapy

Where Context Therapeutics is headquartered

Location

Headquarters

HQ city
Philadelphia
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Context Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Others

Revenue model

  1. No Commercial Revenue: Context Therapeutics is a clinical-stage biopharmaceutical company with no commercialized products and no current revenue. All product candidates are investigational and have not received regulatory approval. Revenue will depend on successful development and commercialization of its bispecific antibody pipeline.

Distribution channels2 records

Marketing channels4 records

Context Therapeutics product offering

Product offering

Core offering

Context Therapeutics develops T cell engaging (TCE) bispecific antibody therapies that bridge tumor cells with T cells to drive immune-mediated killing of solid tumor cancers. Its clinical pipeline comprises three investigational candidates: CTIM-76 (Claudin 6 x CD3), CT-95 (Mesothelin x CD3), and CT-202 (Nectin-4 x CD3), all engineered in an IgG format with silenced Fc for functional monovalency and improved safety. All product candidates are investigational and not yet commercially available.

Product overview

Context Therapeutics is a clinical-stage biopharmaceutical company advancing T cell engaging (TCE) bispecific antibody therapies for solid tumors. The company's pipeline consists of three clinical-stage bispecific antibody product candidates: CTIM-76 (Claudin 6 x CD3), CT-95 (Mesothelin x CD3), and CT-202 (Nectin-4 x CD3). These TCEs are engineered antibodies designed to bridge tumor cells with T cells to activate immune-mediated cancer cell killing.

Differentiator

Problem solved

Functional benefit

Brands

  • CTIM-76: CLDN6 x CD3 bispecific antibody for solid tumors
  • CT-95
  • CT-202

Products and services

  • CTIM-76 CTIM-76 is an investigational Claudin 6 (CLDN6) x CD3 bispecific T cell engaging antibody being developed for solid tumors including ovarian, endometrial, testicular, and gastric cancers. It incorporates a highly selective CLDN6 binding arm developed using Integral Molecular's MPS antibody discovery platform, paired with a CD3 binding scFv domain in an IgG format with silenced Fc to drive T cell-mediated tumor cell killing.
  • CT-95 CT-95 is an investigational mesothelin (MSLN) x CD3 bispecific T cell engaging antibody being developed for MSLN-positive solid tumors including mesothelioma, ovarian cancer, pancreatic adenocarcinoma, non-small cell lung cancer, and triple-negative breast cancer. It features moderate-affinity MSLN binding arms designed to overcome shed mesothelin through membrane-proximal antigen binding.
  • CT-202 CT-202 is an investigational Nectin-4 x CD3 bispecific T cell engaging antibody being developed for Nectin-4-positive solid tumors including bladder, non-small cell lung, colorectal, breast, and head and neck cancers. It incorporates BioAtla's Conditionally Active Biologic (CAB) pH-dependent binding technology that drives activity to the tumor microenvironment while minimizing binding to healthy tissues.

Quantifiable outcome

  • 29% confirmed overall response rate in heavily pretreated platinum-resistant ovarian cancer patients (median 7 prior lines of therapy) with 57% disease control rate
  • +4 more outcomes

Companies that use Context Therapeutics

Customer profile

Named customers5 records

Segments2 records

Ideal customer profiles2 records

Context Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Context Therapeutics partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Tyligand BiosciencecoreOEM/ Whitelabel/ Licensing Partner · 25 August 2021Context Therapeutics and Tyligand Bioscience entered into a license agreement in August 2021, granting Tyligand exclusive rights and sole responsibility for development and commercialization of ONA-XR in China, Hong Kong, and Macau. Context retains rest of world rights and is eligible to receive royalties on net sales. Tyligand had previously completed ONA-XR manufacturing process optimization in collaboration with Context.
  • Jefferson HealthminorStrategic or Co-development Partner · 12 May 2021Jefferson Health and Context Therapeutics collaborated on a Phase 2 clinical trial of ONA-XR in advanced endometrial cancer, with Jefferson Health dosing the first patient. Context has since shifted strategic focus to T cell engaging bispecific antibodies (CTIM-76, CT-95, CT-202).
  • Integral MolecularcoreTechnology or IntegrationContext Therapeutics utilized Integral Molecular's MPS (Membrane Protein Scaffold) antibody discovery platform to isolate and optimize rare antibodies against CLDN6 that do not cross-react with other CLDN family members. This platform technology was critical to the development of CTIM-76's highly selective CLDN6 binding arm.
  • BioAtlacoreTechnology or IntegrationCT-202 incorporates BioAtla's Conditionally Active Biologic (CAB) technology that uses pH dependency to drive localized antibody activity to the tumor microenvironment, minimizing binding to healthy tissues.

Scale indicators7 records

Recent moves6 records

Expansion highlights5 records

Context Therapeutics competitors and assessment

Company assessment

Direct peers

  • Janux Therapeutics: Clinical-stage immuno-oncology company developing T cell engager (TCE) bispecific antibodies for solid tumors using its proprietary TRACTr platform. Janux is one of the closest publicly traded pure-play peers to Context's TCE bispecific strategy.
  • Harpoon Therapeutics: Developed T cell engaging trispecific and bispecific antibodies for solid tumors (e.g., HPN328, HPN217) using its TriTAC and ProTriTAC platforms; acquired by Merck for ~$680M in March 2024. Harpoon is a direct comparable and its former CMO (Luke Walker) is on Context's board.
  • Maverick Therapeutics: Developed CONDITIONAL bispecific T cell engagers designed to be activated only in the tumor microenvironment, addressing the same solid-tumor selectivity challenges Context targets with CT-202's CAB technology.
  • Cullinan Oncology: Clinical-stage oncology company developing multiple modalities including TCE bispecifics and immune-engaging antibodies for solid tumors, with a similar profile of small-cap, multi-asset, platform-driven development.
  • CytomX Therapeutics: Clinical-stage oncology company developing Probody therapeutics, including masked T cell engaging bispecifics designed to be activated preferentially in the tumor microenvironment — directly analogous to Context's tumor-selective engineering approaches.
  • Adagene: Clinical-stage immuno-oncology company developing TCE bispecifics using its POWERbody platform for conditional activation in tumors, with overlapping solid-tumor focus areas (including MSLN).
  • MacroGenics: Clinical-stage biopharmaceutical company developing bispecific antibodies for cancer, including DART and TRIDENT platforms. Has multiple solid-tumor bispecific programs and serves as a direct small/mid-cap comparable for Context.

Broad incumbents

  • Amgen: Established biopharmaceutical company and pioneer of the BiTE (bispecific T cell engager) platform, with approved assets Blincyto (CD19 x CD3) and Imdelltra (DLL3 x CD3). Amgen is a broad incumbent with far greater resources and represents the most significant competitive threat in solid-tumor TCEs.
  • Xencor: Clinical-stage company developing engineered antibody therapeutics including bispecifics via its XmAb platform. Xencor is a broad incumbent in bispecific antibody engineering, with multiple partnered and wholly-owned oncology bispecific programs in solid tumors.
  • AstraZeneca: Global biopharmaceutical company with a significant oncology franchise and active bispecific antibody development, including TCEs and tumor-targeted immunotherapies. Represents a broad incumbent competitor and potential strategic acquirer of Context's pipeline.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat3 records

Key risks7 records

Key highlights7 records

Customer concentration

Context Therapeutics social profiles

Digital presence

Context Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Context Therapeutics leadership team

Management profile

Number of profiles

Profiles14 records

Context Therapeutics funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors9 records

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

Context Therapeutics M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Context Therapeutics

What does Context Therapeutics do?

Context Therapeutics develops T cell engaging (TCE) bispecific antibody therapies that bridge tumor cells with T cells to drive immune-mediated killing of solid tumor cancers. Its clinical pipeline comprises three investigational candidates: CTIM-76 (Claudin 6 x CD3), CT-95 (Mesothelin x CD3), and CT-202 (Nectin-4 x CD3), all engineered in an IgG format with silenced Fc for functional monovalency and improved safety. All product candidates are investigational and not yet commercially available.

Is Context Therapeutics a public or private company?

Context Therapeutics is a public company. It is classified as public and is currently operating.

When was Context Therapeutics founded?

Context Therapeutics was founded in 2015. It employs 11 to 50 people.

Where is Context Therapeutics based?

Context Therapeutics is headquartered in Philadelphia, United States, in the North America region.

How does Context Therapeutics make money?

One revenue line is on record: no Commercial Revenue.

Who are Context Therapeutics's main competitors?

Direct peers on record are Janux Therapeutics, Harpoon Therapeutics, Maverick Therapeutics, Cullinan Oncology, CytomX Therapeutics, Adagene and MacroGenics. Broad incumbents are Amgen, Xencor and AstraZeneca.

Does Context Therapeutics have an API?

No public API is recorded for Context Therapeutics.

What industry is Context Therapeutics in?

Context Therapeutics's product category is Oncology Biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAF, Bispecific & Multispecific Antibodies, with a secondary code of HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering). Its NAICS code is 325414 and its SIC code is 2834.

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Live signals
AInvestContext Therapeutics: A Real Milestone, but the Money Is Still a Year of Data AwayContext Therapeutics enrolled the first patient in its Phase 1 trial of CT-202, its third T cell–engaging cancer drug. The company holds $43 million in cash and burns about $9 million per quarter, with first data expected in 2027. A capital raise is likely before the CTIM-76 readout in early 2027.American Banking and Market NewsContext Therapeutics Inc. (NASDAQ:CNTX) Given Average Recommendation of “Moderate Buy” by AnalystsContext Therapeutics shares received a consensus "Moderate Buy" rating from ten analysts, with eight buy, one hold and one sell recommendation, and an average 12-month price target of $6.17. The stock opened at $0.38, at its one-year low, after missing analyst EPS estimates of -$0.15 versus -$0.09.Pharmaceutical TechnologyContext drops bispecific T-cell engager on cost-cutting initiative - Pharmaceutical TechnologyContext Therapeutics has discontinued its development of the bispecific T-cell engager CT-95 due to insufficient data and focus on cost-cutting amid a cash shortage. The company is redirecting resources toward two other pipeline assets, CTIM-76 and CT-202, which are in clinical trials for ovarian, urothelial, colorectal, and breast cancers.YahooEndometrial Cancer Market Share Analysis and Industry Trends (2026-2031) Featuring Merck, Eisai, Karyopharm Therapeutics, Context Therapeutics, Seagen and MoreResearchAndMarkets has published a market analysis forecasting the global endometrial cancer market to reach USD 40.66 billion by 2031, driven by rising prevalence and advances in immunotherapy-chemotherapy combinations. The report highlights that regulatory approvals for checkpoint inhibitors like dostarlimab, pembrolizumab, and durvalumab are reshaping frontline treatment guidelines and increasing demand for biomarker testing.Clinical Trials ArenaContext drops bispecific T-cell engager on cost-cutting initiativeContext Therapeutics terminated development of its bispecific T-cell engager CT-95, citing data that did not meet internal advancement criteria. The company will reallocate resources to its other two assets, CTIM-76 and CT-202, with Phase I trials planned for 2026-2027.FierceBiotechContext scraps bispecific T-cell engager program to extend cash runway deeper into 2027Context Therapeutics has discontinued development of its bispecific T-cell engager CT-95, stopping the phase 1 trial before receiving interim data to extend its cash runway. The company paid $3.7 million for the asset in 2024 and spent $2.9 million on it in the first half of 2026, but with cash falling to $43 million and three assets in development, it decided to cut the program and redirect resources. Context expects initial phase 1a results for its two priority programs, CTIM-76 and CT-202, in the second quarter of 2027.BenzingaContext Therapeutics Stock (CNTX) is Falling After Hours: Here's What's Driving the Move - Context TherapContext Therapeutics Inc. (NASDAQ:CNTX) shares fell 30.45% in after-hours trading on Wednesday after the company reported a second-quarter net loss of $14.6 million, nearly doubling the $8.8 million loss from the prior-year period, with research and development expenses rising to $12.5 million from $7.8 million. The clinical-stage biopharmaceutical company also announced it is discontinuing development of CT-95 to prioritize its CTIM-76 and CT-202 programs, while ending the quarter with $43 million in cash that it expects will fund operations into the fourth quarter of 2027. Year-to-date, CNTX shares have declined over 55%.BioWorldContext Therapeutics advancing CT-202 into clinic in AustraliaContext Therapeutics is advancing CT-202 into a first-in-human trial in Australia after receiving Human Research Ethics Committee approval and TGA notification. The immuno-oncology drug's clinical trial notification was acknowledged by Australia's Therapeutic Goods Administration.GlobeNewswireContext Therapeutics Reports Second Quarter 2026 Operating and Pipeline ProgressContext Therapeutics reported Q2 2026 net loss of $14.6 million and cash of $43.0 million, sufficient to fund operations into Q4 2027. The company prioritized CTIM-76 and CT-202, discontinuing CT-95, with initial clinical readouts expected in Q2 2027.Ticker ReportContext Therapeutics Inc. (NASDAQ:CNTX) Short Interest UpdateContext Therapeutics Inc. (NASDAQ:CNTX) saw its short interest surge 106.5% to 6.63 million shares as of July 15th, with 7.6% of the company's stock now sold short and a short-interest ratio of 1.8 days based on average daily volume.