SymbolINTS
NameINTENSITY THERAPEUTICS, INC.
SectorHEALTH CARE
RegionNorth America
IndustryBiotechnology: Biological Products (No Diagnostic Substances)
Address1 ENTERPRISE DRIVE,SUITE 430, SHELTON, Connecticut, 06484, United States
Telephone203-221-7381
Fax
Email
Websitehttps://www.intensitytherapeutics.com
IncorporationUNDEFINED
Incorporated On
Employees
Fiscal Year
Public Since
ExchangesNASDAQ
Auditor
Audit StatusNOT PROVIDED
Reporting Status
CIK0001567264
Description

Intensity Therapeutics, Inc. is a clinical-stage biotechnology company. The Company is engaged in developing an approach to treat solid tumor cancers. It leverages its DfuseRx technology platform to create proprietary drug formulations. Its product candidates have the potential to induce an adaptive immune response that attacks the injected and non-injected tumors. The Companys lead product candidate, INT230-6, is in development for the treatment of patients with solid tumors, such as sarcoma and breast cancer patients. The Company, through Merck Sharpe & Dohme (Merck), evaluates INT230-6 with pembrolizumab. In addition, it also evaluates the combination INT230-6 with Bristol-Myers Squibbs anti-CTLA-4 antibody, ipilimumab. It also has an agreement with the Ottawa Hospital Research Institute and the Ontario Institute of Cancer Research to study INT230-6 in a randomized controlled neoadjuvant phase II study in women with early-stage breast cancer (the INVINCIBLE study) (NCT04781725).

Additional info from NASDAQ:
Intensity Therapeutics, Inc. is a clinical-stage biotechnology company. The Company is engaged in developing an approach to treat solid tumor cancers. It leverages its DfuseRx technology platform to create proprietary drug formulations. Its product candidates have the potential to induce an adaptive immune response that attacks the injected and non-injected tumors. The Companys lead product candidate, INT230-6, is in development for the treatment of patients with solid tumors, such as sarcoma and breast cancer patients. The Company, through Merck Sharpe & Dohme (Merck), evaluates INT230-6 with pembrolizumab. In addition, it also evaluates the combination INT230-6 with Bristol-Myers Squibbs anti-CTLA-4 antibody, ipilimumab. It also has an agreement with the Ottawa Hospital Research Institute and the Ontario Institute of Cancer Research to study INT230-6 in a randomized controlled neoadjuvant phase II study in women with early-stage breast cancer (the INVINCIBLE study) (NCT04781725).

2026-05-14 12:00

Intensity Therapeutics Recognized with GHP Magazines 2026 Healthcare & Pharmaceutical Award

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2026-05-07 20:10

(30% Negative) INTENSITY THERAPEUTICS, INC. (INTS) Reports Q2 2026 Financial Results

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2026-05-07 20:07

Intensity Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update

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2026-05-07 20:06

Intensity Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update

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2026-04-30 17:08

New Form DEFA14A - INTENSITY THERAPEUTICS, INC. <b>Filed:</b> 2026-04-30 <b>AccNo:</b> 0001567264-26-000036 <b>Size:</b> 1 MB

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2026-04-30 17:07

New Form DEF 14A - INTENSITY THERAPEUTICS, INC. <b>Filed:</b> 2026-04-30 <b>AccNo:</b> 0001567264-26-000035 <b>Size:</b> 2 MB

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2026-04-15 13:15

Intensity Therapeutics Recognized with Pinnacle Award for Excellence in Healthcare Innovation

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2026-03-30 21:29

Director BENDER LEWIS H 🟢 acquired 37.7K shares of INTENSITY THERAPEUTICS, INC. (INTS) at $6.11 Transaction Date: Mar 26, 2026 | Filing ID: 000005

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2026-03-27 20:13

(30% Negative) INTENSITY THERAPEUTICS, INC. (INTS) Reports Q1 2026 Financial Results

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2026-03-27 20:12

Intensity Therapeutics Reports 2025 Year End Financial Results and Highlights, and Provides Corporate Update

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Trial ID Title Phase Indication Status Start Date Completion Date Source
NCT06263231 A Study to Investigate Efficacy & Safety of Intratumoral INT230-6 Compared to U… Phase3 Sarcoma,Soft Tissue Active_Not_Recruiting 2024-06-28 2028-12-01 ClinicalTrials.gov
NCT04781725 INVINCIBLE TRIAL: Intratumoral INT230-6 in Breast Cancer Phase2 Breast Cancer Unknown 2021-03-25 2023-03-01 ClinicalTrials.gov
NCT03058289 A Phase 1/2 Safety Study of Intratumorally Dosed INT230-6 Phase1 Breast Cancer Completed 2017-02-09 2023-02-22 ClinicalTrials.gov
Total clinical trials: 3
Product Name Type Development Stage Therapeutic Area Study Status Trial ID
Saline injection Other Phase PHASE2 Breast Cancer UNKNOWN NCT04781725
INT230-6 Other Phase PHASE2 Breast Cancer UNKNOWN NCT04781725
anti-CTLA-4 antibody Other Phase PHASE1 Breast Cancer COMPLETED NCT03058289
anti-PD-1 antibody Other Phase PHASE1 Breast Cancer COMPLETED NCT03058289
INT230-6 Other Phase PHASE1 Breast Cancer COMPLETED NCT03058289
Pazopanib Other Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Trabectedin Other Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Eribulin Other Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
INT230-6 Other Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Pazopanib DRUG Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Trabectedin DRUG Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Eribulin DRUG Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Saline injection OTHER Phase PHASE2 Breast Cancer UNKNOWN NCT04781725
anti-CTLA-4 antibody BIOLOGICAL Phase PHASE1 Breast Cancer COMPLETED NCT03058289
anti-PD-1 antibody BIOLOGICAL Phase PHASE1 Breast Cancer COMPLETED NCT03058289
INT230-6 DRUG Phase PHASE3 Sarcoma,Soft Tissue ACTIVE_NOT_RECRUITING NCT06263231
Total products: 16