Crossbow Therapeutics
Crossbow Therapeutics is a clinical-stage Cambridge, MA biotech developing T-Bolt™ TCR-mimetic antibody T-cell engagers that target intracellular cancer antigens via peptide-HLA complexes, with lead programs CBX-250 (Phase 1 in AML/MDS) and CBX-663 (pre-IND, TERT-targeted) and revenue expected from future pharmaceutical licensing.
- Company typePrivate
- Founded2023
- HeadquartersCambridge, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Crossbow Therapeutics does
Crossbow Therapeutics is a clinical-stage biotechnology company developing T-cell engager (TCE) immunotherapies that target intracellular cancer proteins presented as peptide-HLA complexes—a class of antigens inaccessible to conventional antibody drugs and existing TCEs that rely on cell-surface proteins. The company's proprietary T-Bolt™ platform combines TCR-mimetic antibody discovery with bispecific T-cell engager architecture, enabling precise targeting of tumor-specific pHLA complexes while maintaining antibody manufacturability.
The pipeline is anchored by CBX-250, a first-in-class bispecific TCE targeting the cathepsin G (CTSG) CG1 pHLA complex for relapsed/refractory AML, HR-MDS, and CMML, which entered a Phase 1 trial (CROSSCHECK-001, NCT06994676) in September 2025. The second program, CBX-663, is a TERT-targeting TCE with dual TERT-binding domains for solid tumor and hematologic malignancies, with an IND filing targeted for Q3 2026. Two earlier-stage programs (CBX-589, CBX-880) extend the pipeline. A strategic collaboration with MD Anderson Cancer Center provides target validation and binder discovery capabilities.
The company is pre-commercial and headquartered in Cambridge, Massachusetts, with revenue expected to derive from future pharmaceutical licensing, co-development deals, milestones, and royalties. It has raised over $157 million across a Series A ($80M, July 2023, led by MPM BioImpact and Pfizer Ventures) and a Series B ($77M, March 2026, co-led by Taiho Ventures and Arkin Bio Capital), with Eli Lilly, Polaris Partners, and BVF Partners as repeat investors and recent additions including Blood Cancer United's Therapy Acceleration Program.
Crossbow Therapeutics firmographics
Firmographics- Name
- Crossbow Therapeutics
- Legal name
- Crossbow Therapeutics, Inc.
- Website
- https://crossbowtx.com
- Company type
- Private
- Founded year
- 2023
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Crossbow Therapeutics is a clinical-stage Cambridge, MA biotech developing T-Bolt™ TCR-mimetic antibody T-cell engagers that target intracellular cancer antigens via peptide-HLA complexes, with lead programs CBX-250 (Phase 1 in AML/MDS) and CBX-663 (pre-IND, TERT-targeted) and revenue expected from future pharmaceutical licensing.
- Ownership category
- akta.pro rank
Crossbow Therapeutics industry classification
Industry- Product category
- Oncology Therapeutics
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414)
- SIC
- Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- Bispecific & Multispecific Antibodies (HLAAAAAF)
Keywords
Where Crossbow Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Cambridge
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Crossbow Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
Revenue model
- Pharmaceutical Licensing and Co-development: Pre-commercial biotech company generating revenue through licensing agreements, co-development partnerships, and milestone payments with pharmaceutical companies. Revenue will be generated from drug development milestones, regulatory approvals, and potential future product sales upon FDA approval.
- Strategic Collaborations: Revenue generated through strategic collaborations with academic institutions and pharmaceutical partners such as MD Anderson Cancer Center, where Crossbow licenses technologies and co-develops therapeutic candidates.
Go-to-market motion1 record
Distribution channels3 records
Marketing channels5 records
Crossbow Therapeutics product offering
Product offeringCore offering
Crossbow Therapeutics develops TCR-mimetic antibody T-cell engager (TCE) immunotherapies for cancer using its proprietary T-Bolt™ platform. The platform engineers bispecific antibodies that recognize intracellular cancer antigens displayed as peptide-HLA complexes on tumor cell surfaces, expanding the target universe beyond what conventional antibodies and existing TCEs can reach. Lead clinical-stage candidates include CBX-250 (cathepsin G-targeting TCE) and CBX-663 (TERT-targeting TCE), with multiple additional pipeline programs.
Product overview
Crossbow Therapeutics is developing T-Bolt™, a proprietary TCR-mimetic antibody technology platform that enables the development of T-cell engager (TCE) immunotherapies targeting intracellular cancer proteins. The company's lead product is CBX-250, a first-in-class TCE targeting Cathepsin G pHLA currently in Phase 1 trials for myeloid malignancies. CBX-663, a second TCE targeting TERT pHLA for solid and hematologic tumors, is advancing toward IND filing. Additional pipeline programs include CBX-589 (Cathepsin G target) and CBX-880 (undisclosed solid tumor target).
Differentiator
Problem solved
Functional benefit
Brands
- T-Bolt™: Proprietary TCR-mimetic antibody technology platform enabling targeting of intracellular cancer antigens for development of T-cell engager therapies.
- CROSSCHECK-001
Products and services
- CBX-250 First-in-class bispecific T-cell engager (TCE) targeting the cathepsin G (CTSG) peptide-HLA (pHLA) complex (HLA-A*02:01-restricted), abundantly expressed on leukemic cells but not on normal myeloid cells. In development for relapsed or refractory myeloid malignancies including acute myeloid leukemia (AML), high-risk myelodysplastic syndrome (HR-MDS), chronic myelomonocytic leukemia (CMML), and chronic myeloid leukemia (CML). Currently in Phase 1 clinical trial (CROSSCHECK-001, NCT06994676).
- CBX-663 Bispecific T-cell engager targeting the telomerase reverse transcriptase (TERT) peptide-HLA complex (HLA-A*02:01-restricted TERT540 peptide). Contains two binding domains for TERT to enhance tumor cell engagement and immune activation. In development for multiple hematologic and solid tumors including squamous non-small cell lung cancer (sqNSCLC), head and neck squamous cell carcinoma (HNSCC), ovarian cancer, esophageal cancer, and others. TERT is expressed in up to 95% of cancers. IND filing projected for Q3 2026.
- CBX-589 Pipeline program also targeting the Cathepsin G peptide-HLA complex, in discovery/early development stage.
- CBX-880 Pipeline program with undisclosed target for solid tumor and hematologic malignancies, in discovery stage.
Quantifiable outcome
- CBX-250 demonstrated high tumor antigen selectivity and potent antileukemic activity in preclinical in vivo models
- +3 more outcomes
Companies that use Crossbow Therapeutics
Customer profileNamed customers1 record
Segments3 records
Ideal customer profiles3 records
Crossbow Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature4 records
Crossbow Therapeutics partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- The University of Texas MD Anderson Cancer CenterflagshipStrategic collaboration for discovery and preclinical development of CBX-250. Gheath Alatrash, DO, PhD, and Jeffrey Molldrem, MD, led discovery and validation of the CTSG-derived peptide (CG1) via functional studies and mass spectrometry. MD Anderson's ORBIT platform within Therapeutics Discovery division developed the TCR-mimetic binder to the CG1 pHLA complex, which Crossbow licensed for development. Crossbow designed and is conducting the CROSSCHECK-001 clinical study.
Scale indicators5 records
Recent moves6 records
Expansion highlights6 records
Crossbow Therapeutics competitors and assessment
Company assessmentDirect peers
- Harpoon Therapeutics: Harpoon developed T-cell engagers (TriTAC platform) for oncology and was acquired by Merck in 2024. It serves as a direct historical peer for bispecific T-cell engager biotechs of similar stage and approach to Crossbow.
- Immunocore: Immunocore is a commercial-stage biotech developing TCR-based immunotherapies for cancer and infectious disease, including the approved TCR therapeutic tebentafusp. It is the most directly comparable peer to Crossbow as both companies engineer TCR-based or TCR-mimetic molecules targeting peptide-HLA complexes for oncology.
- Adaptimmune Therapeutics: Adaptimmune develops engineered TCR-T cell therapies for solid tumors, including the approved afami-cel. It is a direct peer in the TCR-based oncology space and competes for similar target classes and HLA-restricted indications as Crossbow's TCR-mimetic programs.
- Immatics: Immatics develops TCR-based immunotherapies and TCR-mimetic antibody products (e.g., ACTengine and TCER formats) targeting intracellular cancer antigens presented on HLA. Its bispecific TCER pipeline most closely mirrors Crossbow's T-Bolt™ T-cell engager approach.
- Maverick Therapeutics: Maverick developed conditionally active T-cell engagers (COBRA platform) for solid tumors and was acquired by Takeda. It is a direct peer to Crossbow in next-generation bispecific T-cell engager development for oncology.
Broad incumbents
- Macrogenics: Macrogenics develops bispecific antibodies and DART-platform T-cell engagers for oncology (e.g., vobramitamab duocarmazine). It is a broader incumbent operating in the same T-cell engager / bispecific antibody category as Crossbow.
- Amgen: Amgen commercializes Blincyto (blinatumomab), the leading BiTE-format bispecific T-cell engager, and operates broadly in oncology biologics. It is a broad incumbent setting the commercial and clinical benchmark against which Crossbow's T-cell engager programs will be evaluated.
- Genmab: Genmab is a leading bispecific antibody platform company behind the approved Epkinly (epcoritamab) and multiple DuoBody-based oncology programs. It is a broad incumbent in the bispecific antibody space that Crossbow competes within for partnerships and pipeline priority.
- Regeneron: Regeneron has a deep bispecific antibody pipeline (e.g., linvoseltamab, odronextamab) and is a broad incumbent in antibody-based oncology therapeutics. It is comparable to Crossbow as a competitor and potential partner/strategic acquirer in the bispecific antibody space.
Emerging players
- Cullinan Oncology: Cullinan Oncology is a clinical-stage biotech developing targeted oncology therapeutics including T-cell engager and immune-engager programs. It is an emerging player with overlapping modality focus to Crossbow's TCE pipeline.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks7 records
Key highlights7 records
Customer concentration
Crossbow Therapeutics social profiles
Digital presenceCrossbow Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Crossbow Therapeutics leadership team
Management profileNumber of profiles
Profiles16 records
Crossbow Therapeutics funding detail
Funding detailFunding overview
Funding rounds3 records
Investors15 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Crossbow Therapeutics M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Crossbow Therapeutics
What does Crossbow Therapeutics do?
Crossbow Therapeutics develops TCR-mimetic antibody T-cell engager (TCE) immunotherapies for cancer using its proprietary T-Bolt™ platform. The platform engineers bispecific antibodies that recognize intracellular cancer antigens displayed as peptide-HLA complexes on tumor cell surfaces, expanding the target universe beyond what conventional antibodies and existing TCEs can reach. Lead clinical-stage candidates include CBX-250 (cathepsin G-targeting TCE) and CBX-663 (TERT-targeting TCE), with multiple additional pipeline programs.
Is Crossbow Therapeutics a public or private company?
Crossbow Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.
When was Crossbow Therapeutics founded?
Crossbow Therapeutics was founded in 2023. It employs 11 to 50 people.
Where is Crossbow Therapeutics based?
Crossbow Therapeutics is headquartered in Cambridge, United States, in the North America region.
How does Crossbow Therapeutics make money?
Two revenue lines are on record. Pharmaceutical Licensing and Co-development is the primary driver. The others are strategic Collaborations.
Who are Crossbow Therapeutics's main competitors?
Direct peers on record are Harpoon Therapeutics, Immunocore, Adaptimmune Therapeutics, Immatics and Maverick Therapeutics. Broad incumbents are Macrogenics, Amgen, Genmab and Regeneron. Cullinan Oncology is listed as an emerging player.
Does Crossbow Therapeutics have an API?
No public API is recorded for Crossbow Therapeutics.
What industry is Crossbow Therapeutics in?
Crossbow Therapeutics's product category is Oncology Therapeutics. Its primary akta.pro industry code is HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 325414 and its SIC code is 2836.