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NEUROSCOPE INC.

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Company Details

Name: NEUROSCOPE INC.
Jurisdiction: New York
Legal type: DOMESTIC BUSINESS CORPORATION
Status: Active
Date of registration: 28 Mar 2022 (3 years ago)
Entity Number: 6441401
ZIP code: 10583
County: Westchester
Place of Formation: New York
Address: 46 Candlewood Road, Scarsdale, NY, United States, 10583
Principal Address: Jeiran Choupan, 46 Candlewood Road, Scarsdale, NY, United States, 10583

Shares Details

Shares issued 10000

Share Par Value 0.01

Type PAR VALUE

DOS Process Agent

Name Role Address
JEIRAN CHOUPAN DOS Process Agent 46 Candlewood Road, Scarsdale, NY, United States, 10583

Chief Executive Officer

Name Role Address
JEIRAN CHOUPAN Chief Executive Officer 46 CANDLEWOOD ROAD, SCARSDALE, NY, United States, 10583

Unique Entity ID

A UEI is a government-provided number, like a tax ID number, that’s used to identify businesses eligible for federal grants, awards and contracts.

Note: In April 2022, the federal government replaced its old identifier of choice, the Data Universal Numbering System (DUNS) number, with a government-issued UEI. Now all the federal government’s Integrated Award Environment systems use UEI numbers instead of DUNS numbers. So any entity doing business with the federal government must register for a UEI.

Unique Entity ID:
TAKEXWCLRSA8
CAGE Code:
8MZT9
UEI Expiration Date:
2026-01-07

Business Information

Activation Date:
2025-01-09
Initial Registration Date:
2020-06-26

History

Start date End date Type Value
2022-03-28 2024-03-04 Shares Share type: PAR VALUE, Number of shares: 10000, Par value: 0.01

Filings

Filing Number Date Filed Type Effective Date
240304001036 2024-03-04 BIENNIAL STATEMENT 2024-03-04
220328001250 2022-03-28 CERTIFICATE OF INCORPORATION 2022-03-28

USAspending Awards / Financial Assistance

Date:
2024-07-24
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
DEVELOPMENT OF PERIVASCULAR SPACE MAPPING TOOLSET AS A DIAGNOSTIC AID FOR ALZHEIMER'S DISEASE - PROJECT SUMMARY ALZHEIMER’S DISEASE (AD) IS A DEVASTATING DISEASE THAT AFFECTS MILLIONS OF AMERICANS AND IMPOSES A HUGE SOCIO- ECONOMIC BURDEN. AD-RELATED COGNITIVE DECLINE IS ASSOCIATED WITH THE ACCUMULATION OF AMYLOID PLAQUES AND TAU TANGLES, WHICH ARE INSUFFICIENTLY CLEARED BY BRAIN CLEARANCE PATHWAYS. PERIVASCULAR SPACE (PVS) CLEARANCE HEALTH PLAYS A SUBSTANTIAL ROLE IN THE NET CLEARANCE OF METABOLIC WASTE FROM THE BRAIN. HUMAN MAGNETIC RESONANCE IMAGING (MRI) STUDIES HAVE SHOWN THAT THE INTEGRITY OF THE PVS, IS A MARKER OF BRAIN CLEARANCE HEALTH AND ITS ALTERATION IS AN IMPORTANT FEATURE OF AD PATHOLOGY. ANOTHER IMPORTANT CLINICAL RELEVANCE OF PVS IN AD HAS BEEN EMERGED BY THE INTRODUCTION OF THE FIRST CLASSES OF AMYLOID CLEARING TREATMENTS (E.G., BIOGEN:ADUHELM OR EISAI:LECANEMAB). ALZHEIMER’S PATIENTS WITH CEREBRAL AMYLOID ANGIOPATHY COMORBIDITY HAVE HIGH LIKELIHOOD OF MANIFESTING AN ADVERSE EVENT CALLED, AMYLOID RELATED IMAGING ABNORMALITIES (ARIA). PVS IS A DIAGNOSTIC CRITERION FOR CEREBRAL AMYLOID ANGIOPATHY (BASED ON BOSTON CRITERIA 2.0). AD PATIENTS ARE REQUIRED TO GO THROUGH MRI BEFORE AND DURING THE TREATMENT FOR ARIA MONITORING AND PVS ASSESSMENT IS AN INTEGRAL PART OF THE MONITORING. PVS INTEGRITY IS THEREFORE AN IMPORTANT CLINICAL FEATURE IN ALZHEIMER’S DISEASE AND VASCULAR DEMENTIA. HENCE, A TOOL THAT ALLOWS NON-INVASIVE IN-VIVO MAPPING OF PVS FROM CLINICAL MRI IS OF HIGH SIGNIFICANCE TO AID AD DIAGNOSIS AND DISEASE MONITORING. SUCH TOOL, HOWEVER, DOES NOT EXIST. CURRENT CLINICAL ROUTINE TO INVESTIGATE PVS IS BASED ON COUNTING TOTAL NUMBER OF OBSERVED PVS IN MRI BY NEURO-RADIOLOGISTS, WHICH IS NON-SPECIFIC, RATER-DEPENDENT, AND DOES NOT CAPTURE THE DISTRIBUTION, WHOLE EXTENT OF PVS CHANGE NOR VOLUMETRIC FEATURES OF THE PVS. IN PRACTICE, THIS TECHNIQUE IS TIME CONSUMING AND LABORIOUS. THESE LIMITATIONS IN PART HAVE PREVENTED NEUROLOGISTS FROM ADOPTING PVS QUANTIFICATION INTO THEIR CLINICAL ROUTINE. NEUROSCOPE HAS DEVELOPED COMPUTATIONAL TECHNIQUES FOR MAPPING AND QUANTIFYING PVS MORPHOLOGY FROM MRI, WHICH ENABLES AUTOMATED AND ACCURATE QUANTIFICATION OF PVS ACROSS THE BRAIN WITHOUT THE NEED FOR TIME CONSUMING MANUAL INTERVENTION. NEUROSCOPE TOOLS WERE CLINICALLY AND TECHNICALLY VALIDATED (PHASE-I-STTR DELIVERABLES), WITH >99.8% TEST-RETEST RELIABILITY, SENSITIVITY, AND SPECIFICITY OF >98% AND >93%, RESPECTIVELY. OUR PATENT APPLICATION ON OUR TOOLS WAS ALSO SUBMITTED IN FEB 2021 AND THEIR EXECUTABLE STABLE VERSION HAVE BEEN IMPLEMENTED ON OUR CLOUD SERVER. NEUROSCOPE IS NOW READY TO BUILD THE COMMERCIAL ECOSYSTEM THAT ENABLES INTERACTION WITH POTENTIAL CUSTOMERS. THE GOAL OF THIS PROPOSAL IS TO DEVELOP THE IT INFRASTRUCTURE REQUIRED TO COMMERCIALIZE OUR PVS MAPPING TECHNOLOGIES AND TO SUBMIT FDA 510(K) APPLICATION. OUR MAIN CUSTOMERS ARE PHARMACEUTICAL COMPANIES AND HOSPITAL RADIOLOGY SECTORS. THE IT INFRASTRUCTURE IS REQUIRED TO PROVIDE SERVICE IN CLINICAL TRIALS AND THE FDA APPROVAL IS REQUIRED TO EXPAND OUR MARKET DOMAIN TO CLINICAL DIAGNOSTICS. NEUROSCOPE HAS IDENTIFIED POTENTIAL CUSTOMERS AND HAVE ALREADY MADE SIGNIFICANT PROGRESS. SEVERAL INDUSTRY LEADING COMPANIES SHOWN INTEREST IN OUR TECHNOLOGY.
Obligated Amount:
1193370.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00
Date:
2023-09-22
Awarding Agency Name:
Department of Health and Human Services
Transaction Description:
DEVELOPMENT OF PERIVASCULAR SPACE MAPPING TOOLSET AS A DIAGNOSTIC AID FOR ALZHEIMER'S DISEASE - PROJECT SUMMARY ALZHEIMER’S DISEASE (AD) IS A DEVASTATING DISEASE THAT AFFECTS MILLIONS OF AMERICANS AND IMPOSES A HUGE SOCIO- ECONOMIC BURDEN. AD-RELATED COGNITIVE DECLINE IS ASSOCIATED WITH THE ACCUMULATION OF ASS (AMYLOID BETA) PLAQUES AND NEUROFIBRILLARY TANGLES OF HYPERPHOSPHORYLATED TAU PROTEIN, WHICH ARE INSUFFICIENTLY CLEARED AND DEGRADED BY MECHANISMS SUCH AS THE GLIA-LYMPHATIC SYSTEM OR BY TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER (BBB). ANIMAL RESEARCH HAS SHOWN THAT THE GLIA-LYMPHATIC PATHWAY PLAYS A SUBSTANTIAL ROLE IN THE NET CLEARANCE OF ASS. IN ADDITION, REDUCTION OF INTERSTITIAL FLUID EFFLUX TO THE CEREBROSPINAL FLUID, OR REDUCTION OF TRANSPORT ACROSS THE BBB, COULD LESSEN THE ASS CLEARANCE. HUMAN MAGNETIC RESONANCE IMAGING (MRI) STUDIES HAVE ALSO SHOWN THAT THE INTEGRITY OF THE PERIVASCULAR SPACE (PVS), THE PATHWAY OF GLIA-LYMPHATIC SYSTEM, IS A MARKER OF GLIA-LYMPHATIC BRAIN HEALTH AND ITS ALTERATION IS AN IMPORTANT FEATURE OF AD PATHOLOGY. PVS ALTERATION IN AD HAS BEEN SHOWN TO BE INDEPENDENT OF AMYLOID UPTAKE, IMPLICATING ASTROGLIAL INVOLVEMENT SPECIFIC TO AD. INFORMATION ABOUT PVS INTEGRITY COULD ASSIST CLINICIANS WITH MAKING SPECIFIC DIAGNOSIS ABOUT PATIENTS AD STATUS AND MECHANISM. THEREFORE, A TOOL THAT ALLOWS NON-INVASIVE IN-VIVO MAPPING OF PVS FROM CLINICAL MRI IS OF HIGH SIGNIFICANCE TO AID AD DIAGNOSIS AND DISEASE MONITORING BUT DOES NOT YET EXIST. CURRENT CLINICAL ROUTINE TO INVESTIGATE PVS IS A RELATIVELY CRUDE APPROACH BASED ON COUNTING TOTAL NUMBER OF OBSERVED PVS IN MRI BY NEURO-RADIOLOGISTS, WHICH IS NON-SPECIFIC, RATER-DEPENDENT, AND DOES NOT CAPTURE THE DISTRIBUTION, WHOLE EXTENT OF PVS CHANGE NOR VOLUMETRIC FEATURES OF THE PVS. FROM A PRACTICAL POINT OF VIEW, THIS TECHNIQUE IS TIME CONSUMING AND LABORIOUS. THESE LIMITATIONS IN PART HAVE PREVENTED NEUROLOGISTS FROM ADOPTING PVS QUANTIFICATION INTO THEIR CLINICAL ROUTINE. WE HAVE DEVELOPED COMPUTATIONAL TECHNIQUES FOR MAPPING AND QUANTIFYING PVS MORPHOLOGY FROM MRI, WHICH ENABLES AUTOMATED AND ACCURATE QUANTIFICATION OF PVS ACROSS THE BRAIN WITHOUT THE NEED FOR TIME CONSUMING MANUAL INTERVENTION. THESE TECHNIQUES WERE DEVELOPED ON RESEARCH DATA, WHICH HAD SLIGHTLY HIGHER RESOLUTION THAN CLINICAL MRI. THE GOAL OF THIS PROPOSAL IS TO VALIDATE AND OPTIMIZE THIS TECHNOLOGY ON CLINICAL MRI DATA, WHICH CAN BE VARIABLE IN QUALITY AND RESOLUTION. WE ALSO AIM TO DEVELOP A SCANNER- AND HARDWARE-AGNOSTIC DEPLOYABLE ANALYTICAL SOLUTION FOR AUTOMATED PVS QUANTIFICATION, SO THAT PVS MAPPING CAN BE PERFORMED INDEPENDENT OF THE RADIOLOGY/IMAGING IT INFRASTRUCTURE. IF SUCCESSFUL, WE WILL HAVE A FULLY DEVELOPED AND VALIDATED BACKEND SOFTWARE THAT ENABLES AUTOMATED ASSESSMENT OF PVS AND AIDS SPECIFIC AD DIAGNOSIS AND DISEASE MONITORING. UPON THE COMPLETION OF THIS GOAL, OUR PHASE II WILL FOCUS ON TRANSLATION OF THE TECHNOLOGY VIA IMPLEMENTATION AND TESTING OF THE TECHNOLOGY IN COLLABORATION WITH OUR STRATEGIC PARTNERS IN CLINIC (NEURORADIOLOGY DIVISION OF KECK SCHOOL OF MEDICINE), INDUSTRY (BIOGEN INC.) AND RESEARCH (MARKVCID AND NASA). OUR ULTIMATE GOAL WILL BE TO INTEGRATE PVS MEASURES INTO CLINICAL DIAGNOSIS, DISEASE MONITORING AND INTERVENTION EFFICACY ASSESSMENT, AS A SPECIFIC NON-INVASIVE AND IN-VIVO IMAGING MARKER OF AD PATHOLOGY THAT CAN BE AUTOMATICALLY AND RELIABLY MEASURED.
Obligated Amount:
461031.00
Face Value Of Loan:
0.00
Total Face Value Of Loan:
0.00

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Date of last update: 21 Mar 2025

Sources: New York Secretary of State