Official websites use .gov

A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS

A lock ( 🔒 ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Need Help

Assessing the safety and efficacy of SQ3370 in a phase 1b dose-expansion cohort at the recommended Phase 2 dose in patients with advanced sarcoma

Award Number: R44CA265665
ORGANIZATION: NATIONAL CANCER INSTITUTE
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 09/16/2021
PERIOD OF PERFORMANCE END DATE: 02/28/2025

Group Awards By:

View Award Description

Assessing the safety and efficacy of SQ3370 in a phase 1b dose-expansion cohort at the recommended Phase 2 dose in patients with advanced sarcoma - Abstract In 2018, the global incidence of new cancer diagnoses was estimated at over 18 million cases, and cancer- related deaths were estimated at over 9.6 million. Of these cases, the vast majority were solid tumors, accounting for more than 16 million new cases and 8 million cancer deaths. This includes soft tissue sarcoma (STS), a heterogeneous group of aggressive malignant tumors that have a poor 5-year survival rate of only 65%. In the U.S., an estimated 13,000 people will be diagnosed with STS in 2020, and more than 5,000 will die of the disease. For patients diagnosed with STS, treatment often involves chemotherapy with a cytotoxic agent such as doxorubicin (Dox), an anthracycline that has been used to induce tumor regression in a variety of neoplastic conditions. Dox is also known to induce immunogenic cell death and enhance tumor responsiveness to immune checkpoint blockade therapies. Unfortunately, the extended use of Dox in patients is limited by severe toxic side effects—most notably irreversible cardiotoxicity and bone marrow suppression— which can be life threatening. Therefore, there is an immediate need for new methods to reduce the systemic toxicity and off-target effects of Dox while maintaining its antitumor efficacy Shasqi has developed SQ3370, a novel drug product that will improve the treatment of patients with injectable solid tumors undergoing doxorubicin (Dox)-based chemotherapy. Preclinical studies done to-date have shown that SQ3370 results in significant inhibition of tumor growth (both injected and non-injected tumors), immune activation, prolonged survival, and protection against tumor rechallenge, while exhibiting reduced systemic side effects compared to conventional Dox. Extensive preclinical data with SQ3370 has led to an open investigational new drug (IND) application with the U.S. Food and Drug Administration (FDA). A Phase 1, first- in-human, dose-escalation study is currently enrolling to evaluate the safety/tolerability, pharmacokinetics, and preliminary efficacy of SQ3370 in patients with locally advanced or metastatic solid tumors. This Direct to Phase II application seeks to expand this trial once the recommended Phase 2 dose (RP2D) has been reached by adding a dose expansion cohort of 30 patients with soft-tissue sarcoma using a Simon two-stage design. The aims of this project are to assess 1) safety/tolerability and 2) efficacy of SQ3370 in this cohort to determine if the study should proceed to a Phase 2 clinical trial. These aims will accelerate development of SQ3370, a novel therapy that promises to ultimately result in improved treatment and outcomes for millions of patients with solid tumors.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2025 ( Subtotal = $0 )
2025	2024	SHASQI INC	665 3RD ST	SAN FRANCISCO	CA	94107	SAN FRANCISCO	USA	Cancer Treatment Research	000	3	7/3/2025	NON-COMPETING CONTINUATION	$0
														Subtotal = $0

Issue Date FY: 2024 ( Subtotal = $322,142 )
2024	2024	SHASQI INC	665 3RD ST	SAN FRANCISCO	CA	94107	SAN FRANCISCO	USA	Cancer Treatment Research	000	3	3/18/2024	NON-COMPETING CONTINUATION	$322,142
														Subtotal = $322,142

Issue Date FY: 2023 ( Subtotal = $298,843 )
2023	2023	SHASQI INC	665 3RD ST	SAN FRANCISCO	CA	94107	SAN FRANCISCO	USA	Cancer Treatment Research	000	2	3/24/2023	NON-COMPETING CONTINUATION	$298,843
														Subtotal = $298,843

Issue Date FY: 2022 ( Subtotal = $0 )
2022	2021	SHASQI, INC.	665 3RD ST STE 535	SAN FRANCISCO	CA	94107	SAN FRANCISCO	USA	Cancer Treatment Research	000	1	9/9/2022	NEW	$0
														Subtotal = $0

Issue Date FY: 2021 ( Subtotal = $1,376,786 )
2021	2021	SHASQI, INC.	665 3RD ST STE 535	SAN FRANCISCO	CA	94107	SAN FRANCISCO	USA	Cancer Treatment Research	000	1	9/16/2021	NEW	$1,376,786
														Subtotal = $1,376,786

Grand Total All Awards = $1,997,771

Top

All Categories

About

Search

Reports

Data Submission

Award Information

Assessing the safety and efficacy of SQ3370 in a phase 1b dose-expansion cohort at the recommended Phase 2 dose in patients with advanced sarcoma

Award Number: R44CA265665

ORGANIZATION: NATIONAL CANCER INSTITUTE

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 09/16/2021

PERIOD OF PERFORMANCE END DATE: 02/28/2025

Federal Websites

Department of Health & Human Services

HHS Operating Divisions

HHS Staff Divisions

Download A Document Viewer