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BOND BIOSCIENCES, INC.

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Company Details

Name: BOND BIOSCIENCES, INC.
Jurisdiction: New York
Legal type: FOREIGN BUSINESS CORPORATION
Status: Active
Date of registration: 31 Aug 2016 (9 years ago)
Entity Number: 5001586
ZIP code: 10005
County: New York
Place of Formation: Delaware
Address: 28 LIBERTY ST., NEW YORK, NY, United States, 10005
Principal Address: 170 English Landing Drive, SUITE 201B, Parkville, MO, United States, 64152

Agent

Name Role Address
C T CORPORATION SYSTEM Agent 28 LIBERTY ST., NEW YORK, NY, 10005

Chief Executive Officer

Name Role Address
MICHAEL RILEY Chief Executive Officer 170 ENGLISH LANDING DRIVE, SUITE 201B, PARKVILLE, MO, United States, 64152

DOS Process Agent

Name Role Address
C T CORPORATION SYSTEM DOS Process Agent 28 LIBERTY ST., NEW YORK, NY, United States, 10005

History

Start date End date Type Value
2024-08-07 2024-08-07 Address 170 ENGLISH LANDING DRIVE, SUITE 201B, PARKVILLE, MO, 64152, USA (Type of address: Chief Executive Officer)
2024-08-07 2024-08-07 Address 6228 NORTHLAKE DR, PARKVILLE, MO, 64152, USA (Type of address: Chief Executive Officer)
2020-08-03 2024-08-07 Address 28 LIBERTY ST., NEW YORK, NY, 10005, USA (Type of address: Service of Process)
2019-01-28 2020-08-03 Address 28 LIBERTY ST., NEW YORK, NY, 10005, USA (Type of address: Service of Process)
2019-01-28 2024-08-07 Address 28 LIBERTY ST., NEW YORK, NY, 10005, USA (Type of address: Registered Agent)

Filings

Filing Number Date Filed Type Effective Date
240807000765 2024-08-07 BIENNIAL STATEMENT 2024-08-07
220915002502 2022-09-15 BIENNIAL STATEMENT 2022-08-01
200803061223 2020-08-03 BIENNIAL STATEMENT 2020-08-01
SR-76350 2019-01-28 CERTIFICATE OF CHANGE (BY AGENT) 2019-01-28
SR-76349 2019-01-28 CERTIFICATE OF CHANGE (BY AGENT) 2019-01-28

USAspending Awards / Financial Assistance

Date:
2021-07-15
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
PREPARING BBI-001 AS AN ORAL, NON-ABSORBED IRON CHELATOR FOR PREVENTION OF IRON OVERLOAD - PROJECT SUMMARY/ABSTRACT HEREDITARY HEMOCHROMATOSIS (HH) IS ONE OF THE MOST COMMON GENETIC DISORDERS IN THE UNITED STATES AFFECTING 1 MILLION PEOPLE PRIMARILY OF NORTHERN EUROPEAN DESCENT. PEOPLE WITH HH ARE UNABLE TO PRODUCE HEPCIDIN AND, AS A RESULT, EXPERIENCE EXCESS ABSORPTION OF DIETARY IRON. EXCESS IRON IS STORED IN TISSUES AND ORGANS, CAUSING CLINICAL IRON OVERLOAD AND SEVERE HEALTH ISSUES, INCLUDING CIRRHOSIS AND HEART FAILURE. PHLEBOTOMY IS THE PRIMARY TREATMENT FOR MANAGING SERUM FERRITIN LEVELS IN PATIENTS WITH HH, WITH PATIENTS REQUIRING MAINTENANCE PHLEBOTOMY TREATMENTS 4-6 TIMES PER YEAR ON AVERAGE THROUGHOUT THEIR LIFETIME. WHILE PHLEBOTOMY IS SAFE, IT IS NOT WELL TOLERATED BY PATIENTS. THIS LEADS TO POOR LONG-TERM COMPLIANCE, SIGNIFICANT ORGAN DAMAGE, AND INCREASED RISK OF SEVERE HEALTH CONDITIONS. PHARMACOLOGIC TREATMENT OFFERS AN ATTRACTIVE ALTERNATIVE TO MAINTENANCE PHLEBOTOMY. HOWEVER, WHILE STUDIES HAVE EXPLORED THE POTENTIAL OF PHARMACOLOGIC INTERVENTIONS FOR IRON OVERLOAD (E.G., SYSTEMIC IRON CHELATION THERAPY, PROTEIN REPLACEMENT THERAPY, GENE THERAPY), FEW HAVE BEEN CLINICALLY TRANSLATED AND NONE HAVE BEEN COMMERCIALIZED FOR CHRONIC MANAGEMENT OF IRON OVERLOAD DUE TO ISSUES OF SAFETY AND COST. AS A RESULT, THERE IS A SIGNIFICANT NEED FOR A SAFE, CONVENIENT INTERVENTION THAT IS AN EFFECTIVE ALTERNATIVE TO PHLEBOTOMY FOR CHRONIC MAINTENANCE OF IRON OVERLOAD IN PATIENTS WITH HH. IN THIS PROJECT, WE WILL DEVELOP AN ORALLY DOSED, NON-ABSORBED IRON CHELATOR, BBI-001, THAT BINDS DIETARY IRON IN THE SMALL INTESTINE AND ELIMINATES IT THROUGH FECAL OUTPUT FOR CHRONIC MAINTENANCE OF SERUM FERRITIN LEVELS IN PATIENTS WITH HH. PRELIMINARY STUDIES OF BBI-001 HAVE VALIDATED ITS MECHANISM OF ACTION IN A SMALL ANIMAL MODEL AND DEMONSTRATED THAT IT IS NON-ABSORBED AND HAS HIGH IRON BINDING CAPACITY, AND SELECTIVITY WITH RAPID KINETICS FOR BINDING IRON PRIOR TO ABSORPTION IN THE GASTROINTESTINAL TRACT. THIS PHASE I SBIR STUDY HAS TWO SPECIFIC AIMS: IN SPECIFIC AIM 1, WE WILL COMPLETE A PRECLINICAL MAXIMUM TOLERATED DOSE TOXICITY STUDY IN RATS TO VALIDATE BBI-001’S SAFETY WHEN MULTIPLE DOSES ARE GIVEN PER DAY. SPECIFIC AIM 2 WILL FOCUS ON RAPID CLINICAL TRANSLATION OF BBI-001 BY PREPARING A PACKAGE TO SUPPORT A PRE-IND (INVESTIGATIONAL NEW DRUG) MEETING WITH THE FDA FOR BBI-001 AND BY ADVANCING CHEMISTRY, MANUFACTURING, AND CONTROLS (CMC) STRATEGY IN PREPARATION FOR CGMP PRODUCTION. THE LONG-TERM GOAL OF THIS PROJECT IS TO COMMERCIALIZE BBI-001 AS THE FIRST AND ONLY NON- TOXIC IRON CHELATION THERAPY AND A SAFE AND EFFECTIVE ALTERNATIVE TO MAINTENANCE PHLEBOTOMY FOR CHRONIC MAINTENANCE OF SERUM FERRITIN LEVELS IN HH PATIENTS. CHRONIC TREATMENT OF IRON OVERLOAD IN HH PATIENTS WITH BBI-001 WILL RESULT IN IMPROVED COMPLIANCE AND MORE CONSISTENT MAINTENANCE OF SERUM FERRITIN LEVELS, LEADING TO LOWER RISK OF ORGAN DAMAGE AND RELATED COMPLICATIONS, REDUCED HEALTHCARE COSTS, AND IMPROVED LONG-TERM OUTCOMES IN PATIENTS WITH HH.
Obligated Amount:
299359.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00

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Date of last update: 24 Mar 2025

Sources: New York Secretary of State