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Vascarta

Full company profile

uuid00025tg

Namestring
Vascarta
Legal namestring
Vascarta Inc.
Websiteurl
vascarta.com
Company typeenum
Private
Founded yearint
2020
Descriptiontext

Vascarta is a clinical-stage pharmaceutical company developing transdermal drug delivery treatments for chronic inflammatory diseases, with lead candidate VAS-101 (Vasceptor®) — a topical curcumin gel — advancing in Phase 1 trials for sickle cell disease and knee osteoarthritis. The company is built on two proprietary technology pillars: Vasporta™, a patented transdermal delivery system that bypasses the well-documented poor oral bioavailability of curcumin and offers a needle-free alternative to injections, and Vasceptor®, a curcumin-based formulation that demonstrates systemic therapeutic effect via red blood cell distribution. Beyond the lead asset, Vascarta has expanded its pipeline through an exclusive license to CUNY's novel oncology linker chemistry, producing preclinical candidates STO-1 (glioblastoma) and STO-2 (curcumin-Gemzar conjugate).

The company currently generates no commercial revenue; VAS-101 is distributed on a prescription basis exclusively through Town & Country Compounding Pharmacy in Ramsey, NJ, which is licensed to dispense to 22 U.S. states, while insurance coverage for compounded products is typically absent and pricing is not publicly disclosed. Primary patient populations are sickle cell disease patients (FDA Orphan Drug Designation received) and osteoarthritis patients (approximately 32.5 million U.S. adults and 500 million globally). Strategic partnerships include the NHLBI/NIH for the SCD Phase 1 study, the Foundation for Sickle Cell Disease Research for clinical trial execution, CUNY for oncology, and the FDA CBER for mechanistic work. Vascarta is headquartered in Summit, New Jersey, was founded in 2020, and is led by Dr. Richard Prince (CEO), Dr. Joel Friedman (CSO), with Richard Serbin (ex-Johnson & Johnson) appointed as Chief Strategy Officer in June 2026.

Short descriptiontext

Vascarta is a clinical-stage pharmaceutical company developing VAS-101, a patented transdermal curcumin gel (Vasporta™/Vasceptor®) for sickle cell disease and osteoarthritis, with an oncology pipeline licensed from CUNY. Pre-revenue; FDA Orphan Drug Designation secured.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersSummit, United States
HQ citystring
Summit
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
transdermal drug delivery, curcumin therapeutics, sickle cell treatment, osteoarthritis therapy, pharmaceutical development
Industry1 code
1Primary Care & General Medicine Pharmaceuticals
CodeHLAIAAAAPrimaryYes
NAICS code1 code
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Transdermal Pharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Vasporta™
Description

Patented transdermal delivery platform technology designed to improve absorption, eliminate the need for injections, and overcome oral bioavailability limitations.

vascarta.com
+1 more record
Core offering1 text field

Vascarta is a clinical-stage pharmaceutical company that develops and markets prescription transdermal curcumin-based treatments (lead candidate VAS-101 / Vasceptor®) for chronic inflammatory diseases, including sickle cell disease and knee osteoarthritis, using its proprietary Vasporta™ transdermal delivery platform. The company also holds an exclusive oncology licensing platform for CUNY-derived linker chemistry drug candidates (STO-1, STO-2) targeting cancers such as glioblastoma and pancreatic cancer.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • VAS-101 users reported 39.3% feeling 'much improved' or 'very much improved' compared with 13.3% in placebo group in osteoarthritis Phase 1b trial (60 patients over 28 days)
+3 more records
Product overview1 text field

Vascarta is a clinical-stage pharmaceutical company built on a proprietary transdermal drug delivery platform (Vasporta™). The company's core product is VAS-101 (also marketed as Vasceptor®), a topical curcumin gel formulation that overcomes the poor oral bioavailability of curcumin through transdermal delivery. VAS-101 is in Phase I clinical trials for both sickle cell disease and knee osteoarthritis. Vascarta also operates an oncology licensing platform through an exclusive agreement with CUNY, developing drug candidates including STO-1 for glioblastoma and STO-2 (curcumin-Gemzar conjugate) for potential transdermal cancer treatment. The company is headquartered in Summit, New Jersey.

Product and service1 record
1VAS-101 (Vasceptor®) Topical Transdermal Curcumin Gel
CategoryPrescription transdermal anti-inflammatory drug
Description

VAS-101 (also marketed as Vasceptor®) is Vascarta's lead product candidate — a prescription-only topical/transdermal curcumin gel that uses the Vasporta™ delivery platform to overcome the poor oral bioavailability of curcumin. It is being developed for sickle cell disease and knee osteoarthritis, with FDA Orphan Drug Designation in the SCD indication. The product is dispensed exclusively through Town & Country Compounding Pharmacy in Ramsey, NJ, licensed to ship to 22 U.S. states.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-03
Description

FDA-led study demonstrated that Vascarta's transdermal curcumin formulation (VAS-101) improved cardiac mitochondrial function in a sickle cell disease mouse model by reducing oxidative stress and enhancing mitochondrial bioenergetics.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-10
Description

Collaboration for preclinical breakthrough in glioblastoma treatment using drug candidate STO-1, which selectively eliminates tumor cells in mice with high survival rate. Also collaborated to improve chemotherapy efficacy and safety through novel linker chemistry.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-01-01
Description

Signed clinical trial agreement with Vascarta to perform Phase 1 clinical study of VAS-101 in sickle cell disease.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Clinical trial partner conducting Phase I pilot clinical trial using Vasceptor® (VAS-101) in individuals with sickle cell disease in Hollywood, Florida, USA. Patients are treated via topical and sublingual routes of administration.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Exclusive pharmacy partner for prescription fulfillment of Vascarta's topical/transdermal curcumin gel formulation. Located in Ramsey, New Jersey, licensed to ship prescription products across 22 U.S. states.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Acquired by Pfizer for $5.4B, GBT developed Oxbryta (voxelotor) for sickle cell disease — the same indication as Vascarta's VAS-101. GBT is the most directly comparable peer for Vascarta's sickle cell disease program and represents a realistic strategic acquirer profile.

TypeBroad incumbent
Description

Vertex developed Casgevy (exa-cel), the first FDA-approved CRISPR gene therapy for sickle cell disease. While operating at much larger scale and with a different mechanism, Vertex is a key competitive and benchmark player in the sickle cell treatment space.

TypeDirect peer
Description

Small-cap commercial-stage company that developed Endari (L-glutamine), an FDA-approved therapy for sickle cell disease. Emmaus is highly comparable as a smaller company focused on sickle cell disease therapeutics and serves as a useful precedent for commercial-scale validation.

TypeDirect peer
Description

Specialty pharmaceutical company focused on novel delivery approaches (e.g., buccal film technology) for pain and addiction. Comparable to Vascarta as a small specialty pharma using alternative drug delivery technologies to commercialize differentiated pain and CNS therapies.

TypeDirect peer
Description

Specialty pharmaceutical company wholly-owned by Hisamitsu, focused on transdermal drug delivery systems. Noven's expertise in patch-based delivery technology makes it a strong comparable for Vascarta's Vasporta™ transdermal platform approach.

TypeEmerging player
Description

Commercial-stage specialty pharma developing therapeutics for pain management and postoperative care. Comparable as a small specialty pharma targeting pain/inflammation markets with novel delivery approaches, though at a more advanced commercial stage.

TypeEmerging player
Description

Clinical-stage biopharma developing novel peripherally acting kappa opioid receptor agonists for chronic pruritus and pain. Comparable to Vascarta as a small clinical-stage company developing differentiated therapies for pain and inflammation.

TypeEmerging player
Description

Clinical-stage pharma focused on non-opioid, non-NSAID treatments for chronic pain conditions including osteoarthritis. Highly comparable target patient population and therapeutic positioning to Vascarta's VAS-101 OA program.

TypeBroad incumbent
Description

Developed Zilretta (triamcinolone acetonide extended-release), an intra-articular therapy for knee osteoarthritis pain. Acquired by Pacira for ~$1B; represents a relevant precedent for successful exits in the OA pain space.

TypeBroad incumbent
Description

Developed Adakveo (crizanlizumab) for vaso-occlusive crisis prevention in sickle cell disease — the same patient population as VAS-101. As a global pharma incumbent in sickle cell, Novartis represents both a competitive threat and a potential strategic acquirer of late-stage sickle cell assets.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Vascarta

Transdermal Pharmaceuticalsvascarta.com

Vascarta is a clinical-stage pharmaceutical company developing VAS-101, a patented transdermal curcumin gel (Vasporta™/Vasceptor®) for sickle cell disease and osteoarthritis, with an oncology pipeline licensed from CUNY. Pre-revenue; FDA Orphan Drug Designation secured.

What Vascarta does

Vascarta is a clinical-stage pharmaceutical company developing transdermal drug delivery treatments for chronic inflammatory diseases, with lead candidate VAS-101 (Vasceptor®) — a topical curcumin gel — advancing in Phase 1 trials for sickle cell disease and knee osteoarthritis. The company is built on two proprietary technology pillars: Vasporta™, a patented transdermal delivery system that bypasses the well-documented poor oral bioavailability of curcumin and offers a needle-free alternative to injections, and Vasceptor®, a curcumin-based formulation that demonstrates systemic therapeutic effect via red blood cell distribution. Beyond the lead asset, Vascarta has expanded its pipeline through an exclusive license to CUNY's novel oncology linker chemistry, producing preclinical candidates STO-1 (glioblastoma) and STO-2 (curcumin-Gemzar conjugate).

The company currently generates no commercial revenue; VAS-101 is distributed on a prescription basis exclusively through Town & Country Compounding Pharmacy in Ramsey, NJ, which is licensed to dispense to 22 U.S. states, while insurance coverage for compounded products is typically absent and pricing is not publicly disclosed. Primary patient populations are sickle cell disease patients (FDA Orphan Drug Designation received) and osteoarthritis patients (approximately 32.5 million U.S. adults and 500 million globally). Strategic partnerships include the NHLBI/NIH for the SCD Phase 1 study, the Foundation for Sickle Cell Disease Research for clinical trial execution, CUNY for oncology, and the FDA CBER for mechanistic work. Vascarta is headquartered in Summit, New Jersey, was founded in 2020, and is led by Dr. Richard Prince (CEO), Dr. Joel Friedman (CSO), with Richard Serbin (ex-Johnson & Johnson) appointed as Chief Strategy Officer in June 2026.

Vascarta firmographics

Firmographics
Name
Vascarta
Legal name
Vascarta Inc.
Website
https://vascarta.com
Company type
Private
Founded year
2020
Operating status
Operating
Headcount range
1–10 employees
Short description
Vascarta is a clinical-stage pharmaceutical company developing VAS-101, a patented transdermal curcumin gel (Vasporta™/Vasceptor®) for sickle cell disease and osteoarthritis, with an oncology pipeline licensed from CUNY. Pre-revenue; FDA Orphan Drug Designation secured.
Ownership category
akta.pro rank

Vascarta industry classification

Industry
Product category
Transdermal Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Primary Care & General Medicine Pharmaceuticals (HLAIAAAA)

Keywords

  • Transdermal drug delivery
  • Curcumin therapeutics
  • Sickle cell treatment
  • Osteoarthritis therapy
  • Pharmaceutical development

Where Vascarta is headquartered

Location

Headquarters

HQ city
Summit
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Vascarta business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Others

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Vascarta product offering

Product offering

Core offering

Vascarta is a clinical-stage pharmaceutical company that develops and markets prescription transdermal curcumin-based treatments (lead candidate VAS-101 / Vasceptor®) for chronic inflammatory diseases, including sickle cell disease and knee osteoarthritis, using its proprietary Vasporta™ transdermal delivery platform. The company also holds an exclusive oncology licensing platform for CUNY-derived linker chemistry drug candidates (STO-1, STO-2) targeting cancers such as glioblastoma and pancreatic cancer.

Product overview

Vascarta is a clinical-stage pharmaceutical company built on a proprietary transdermal drug delivery platform (Vasporta™). The company's core product is VAS-101 (also marketed as Vasceptor®), a topical curcumin gel formulation that overcomes the poor oral bioavailability of curcumin through transdermal delivery. VAS-101 is in Phase I clinical trials for both sickle cell disease and knee osteoarthritis. Vascarta also operates an oncology licensing platform through an exclusive agreement with CUNY, developing drug candidates including STO-1 for glioblastoma and STO-2 (curcumin-Gemzar conjugate) for potential transdermal cancer treatment. The company is headquartered in Summit, New Jersey.

Differentiator

Problem solved

Functional benefit

Brands

  • Vasporta™: Patented transdermal delivery platform technology designed to improve absorption, eliminate the need for injections, and overcome oral bioavailability limitations.
  • Vasceptor®

Products and services

  • VAS-101 (Vasceptor®) Topical Transdermal Curcumin Gel VAS-101 (also marketed as Vasceptor®) is Vascarta's lead product candidate — a prescription-only topical/transdermal curcumin gel that uses the Vasporta™ delivery platform to overcome the poor oral bioavailability of curcumin. It is being developed for sickle cell disease and knee osteoarthritis, with FDA Orphan Drug Designation in the SCD indication. The product is dispensed exclusively through Town & Country Compounding Pharmacy in Ramsey, NJ, licensed to ship to 22 U.S. states.

Quantifiable outcome

  • VAS-101 users reported 39.3% feeling 'much improved' or 'very much improved' compared with 13.3% in placebo group in osteoarthritis Phase 1b trial (60 patients over 28 days)
  • +3 more outcomes

Companies that use Vascarta

Customer profile

Segments3 records

Ideal customer profiles3 records

Vascarta technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Vascarta partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core.

  • FDA Center for Biologics Evaluation and Research (CBER)coreStrategic or Co-development Partner · 3 December 2025FDA-led study demonstrated that Vascarta's transdermal curcumin formulation (VAS-101) improved cardiac mitochondrial function in a sickle cell disease mouse model by reducing oxidative stress and enhancing mitochondrial bioenergetics.
  • CUNY (City University of New York)coreStrategic or Co-development Partner · 10 November 2025Collaboration for preclinical breakthrough in glioblastoma treatment using drug candidate STO-1, which selectively eliminates tumor cells in mice with high survival rate. Also collaborated to improve chemotherapy efficacy and safety through novel linker chemistry.
  • National Heart, Lung, and Blood Institute / National Institutes of Health (NHLBI/NIH)coreStrategic or Co-development Partner · 1 January 2025Signed clinical trial agreement with Vascarta to perform Phase 1 clinical study of VAS-101 in sickle cell disease.
  • Foundation for Sickle Cell Disease Research (FSCDR)coreStrategic or Co-development PartnerClinical trial partner conducting Phase I pilot clinical trial using Vasceptor® (VAS-101) in individuals with sickle cell disease in Hollywood, Florida, USA. Patients are treated via topical and sublingual routes of administration.
  • Town & Country Compounding PharmacycoreChannel Partner/ Reseller/ DistributorExclusive pharmacy partner for prescription fulfillment of Vascarta's topical/transdermal curcumin gel formulation. Located in Ramsey, New Jersey, licensed to ship prescription products across 22 U.S. states.

Scale indicators1 record

Recent moves7 records

Expansion highlights6 records

Vascarta competitors and assessment

Company assessment

Direct peers

  • Global Blood Therapeutics (Pfizer): Acquired by Pfizer for $5.4B, GBT developed Oxbryta (voxelotor) for sickle cell disease — the same indication as Vascarta's VAS-101. GBT is the most directly comparable peer for Vascarta's sickle cell disease program and represents a realistic strategic acquirer profile.
  • Emmaus Life Sciences: Small-cap commercial-stage company that developed Endari (L-glutamine), an FDA-approved therapy for sickle cell disease. Emmaus is highly comparable as a smaller company focused on sickle cell disease therapeutics and serves as a useful precedent for commercial-scale validation.
  • BioDelivery Sciences International: Specialty pharmaceutical company focused on novel delivery approaches (e.g., buccal film technology) for pain and addiction. Comparable to Vascarta as a small specialty pharma using alternative drug delivery technologies to commercialize differentiated pain and CNS therapies.
  • Noven Pharmaceuticals: Specialty pharmaceutical company wholly-owned by Hisamitsu, focused on transdermal drug delivery systems. Noven's expertise in patch-based delivery technology makes it a strong comparable for Vascarta's Vasporta™ transdermal platform approach.

Broad incumbents

  • Vertex Pharmaceuticals: Vertex developed Casgevy (exa-cel), the first FDA-approved CRISPR gene therapy for sickle cell disease. While operating at much larger scale and with a different mechanism, Vertex is a key competitive and benchmark player in the sickle cell treatment space.
  • Flexion Therapeutics (now Pacira BioSciences): Developed Zilretta (triamcinolone acetonide extended-release), an intra-articular therapy for knee osteoarthritis pain. Acquired by Pacira for ~$1B; represents a relevant precedent for successful exits in the OA pain space.
  • Novartis: Developed Adakveo (crizanlizumab) for vaso-occlusive crisis prevention in sickle cell disease — the same patient population as VAS-101. As a global pharma incumbent in sickle cell, Novartis represents both a competitive threat and a potential strategic acquirer of late-stage sickle cell assets.

Emerging players

  • Heron Therapeutics: Commercial-stage specialty pharma developing therapeutics for pain management and postoperative care. Comparable as a small specialty pharma targeting pain/inflammation markets with novel delivery approaches, though at a more advanced commercial stage.
  • Cara Therapeutics: Clinical-stage biopharma developing novel peripherally acting kappa opioid receptor agonists for chronic pruritus and pain. Comparable to Vascarta as a small clinical-stage company developing differentiated therapies for pain and inflammation.
  • Centrexion Therapeutics: Clinical-stage pharma focused on non-opioid, non-NSAID treatments for chronic pain conditions including osteoarthritis. Highly comparable target patient population and therapeutic positioning to Vascarta's VAS-101 OA program.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Vascarta social profiles

Digital presence

Vascarta financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Vascarta leadership team

Management profile

Number of profiles

Profiles8 records

Vascarta funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Vascarta M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Vascarta

What does Vascarta do?

Vascarta is a clinical-stage pharmaceutical company that develops and markets prescription transdermal curcumin-based treatments (lead candidate VAS-101 / Vasceptor®) for chronic inflammatory diseases, including sickle cell disease and knee osteoarthritis, using its proprietary Vasporta™ transdermal delivery platform. The company also holds an exclusive oncology licensing platform for CUNY-derived linker chemistry drug candidates (STO-1, STO-2) targeting cancers such as glioblastoma and pancreatic cancer.

Is Vascarta a public or private company?

Vascarta is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Vascarta founded?

Vascarta was founded in 2020. It employs 1 to 10 people.

Where is Vascarta based?

Vascarta is headquartered in Summit, United States, in the North America region.

Who are Vascarta's main competitors?

Direct peers on record are Global Blood Therapeutics (Pfizer), Emmaus Life Sciences, BioDelivery Sciences International and Noven Pharmaceuticals. Broad incumbents are Vertex Pharmaceuticals, Flexion Therapeutics (now Pacira BioSciences) and Novartis. Emerging players are Heron Therapeutics, Cara Therapeutics and Centrexion Therapeutics.

Does Vascarta have an API?

No public API is recorded for Vascarta.

What industry is Vascarta in?

Vascarta's product category is Transdermal Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAA, Primary Care & General Medicine Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
AijournVascarta Outlines VAS-101’s (Vasceptor®) Potential as a Non-Opioid Advance in Pain Medicine Across Sickle Cell Disease, Osteoarthritis, and CancerVascarta Inc. announced on August 25, 2026 that its lead candidate VAS-101 (Vasceptor), a transdermal curcumin formulation, showed converging preclinical and clinical evidence across sickle cell disease, chemotherapy-induced pain and osteoarthritis. A Phase 1b trial in knee osteoarthritis reported roughly 40% of participants with meaningful pain improvement within 28 days. The company said it expects IND submissions and collaboration work to follow.PR NewswireVascarta Outlines VAS-101's (Vasceptor®) Potential as a Non-Opioid Advance in Pain Medicine Across Sickle Cell Disease, Osteoarthritis, and CancerVascarta outlined preclinical and clinical data for VAS-101 (Vasceptor), a transdermal curcuminoid, targeting a shared IL-17-driven p38 MAPK pain pathway across sickle cell disease, chemotherapy-induced pain, and osteoarthritis. The company cited a Phase 1b trial showing significant pain score reductions in knee osteoarthritis patients versus placebo. It plans to advance IND submissions.BioSpaceVascarta Outlines Proposed Mechanistic Link Between VAS-101’s (Vasceptor®) Vascular and Red Blood Cell Effects in Sickle Cell DiseaseVascarta outlined a proposed mechanism linking VAS-101's vascular and red blood cell effects in sickle cell disease, based on a preclinical study preserving tissue oxygenation and a clinical pilot showing improved sickling kinetics. The company suggests the drug reduces oxidative damage to RBCs, lowering sickling propensity without direct hemoglobin inhibition. It plans to test this hypothesis in future studies.AijournVascarta Outlines Proposed Mechanistic Link Between VAS-101’s (Vasceptor®) Vascular and Red Blood Cell Effects in Sickle Cell DiseaseVascarta Inc. proposed a mechanistic framework linking its drug candidate VAS-101 to improved red blood cell sickling kinetics in sickle cell disease patients, based on preclinical microcirculation data and prior Phase I clinical results. The company suggests that low-dose transdermal or sublingual curcuminoids reduce oxidative stress and preserve tissue oxygenation, thereby interrupting the cycle of hypoxia-induced sickling without directly inhibiting hemoglobin polymerization. This hypothesis aims to support the company's upcoming Investigational New Drug (IND) submission later this year.PR NewswireVascarta Outlines Proposed Mechanistic Link Between VAS-101's (Vasceptor®) Vascular and Red Blood Cell Effects in Sickle Cell DiseaseVascarta Inc. proposed a mechanistic framework linking preclinical findings on tissue oxygenation preservation with clinical data showing improved red blood cell sickling kinetics in SCD patients treated with its drug candidate Vasceptor® (VAS-101). The company suggests that low-dose, repeated exposure to the curcuminoid formulation reduces oxidative stress and inflammatory burden rather than directly inhibiting hemoglobin polymerization, thereby interrupting the cycle of hypoxia and cell damage. This hypothesis aims to guide future studies and supports the company's plan for an IND submission later this year.AijournVascarta Announces NIH Phase I clinical study of VAS-101 in sickle cell disease beginsVascarta Inc. announced that a Phase I clinical study of its VAS-101 topical curcumin gel for sickle cell disease has begun at the National Institutes of Health Clinical Center in the United States. The study, led by Dr. Swee Lay Thein, aims to evaluate the safety and tolerability of escalating doses of the drug in patients with stable sickle cell disease.PR NewswireVascarta Announces NIH Phase I clinical study of VAS-101 in sickle cell disease beginsVascarta Inc. announced the commencement of a second Phase I clinical study for VAS-101, a topical curcumin gel, at the National Institutes of Health (NIH) Clinical Center to evaluate its safety and tolerability in patients with sickle cell disease. The trial, led by Dr. Swee Lay Thein, aims to assess the efficacy of this transdermal delivery technology as a potential new standard of care for managing pain and inflammation associated with the condition.AijournVascarta Announces Phase I Results of VAS-101 Administered Sublingually in Sickle Cell Disease PatientsVascarta Inc. announced successful completion of the sublingual arm of its Phase I clinical trial evaluating VAS-101 (topical curcumin gel) for sickle cell disease, conducted by the Foundation for Sickle Cell Disease Research in Florida with 5 patients over 29 days. All participants demonstrated favorable safety and tolerability with directional improvements in pain scores (7.0 to 6.6), fatigue metrics, and red blood cell functional biomarkers suggesting improved sickling kinetics. The company plans to file an Investigational New Drug Application with the FDA later this year and will evaluate higher doses in future studies.PR NewswireVascarta Announces Phase I Results of VAS-101 Administered Sublingually in Sickle Cell Disease PatientsVascarta Inc. announced successful completion of the sublingual arm of its Phase I clinical trial for VAS-101 (Vasceptor), a topical curcumin formulation being evaluated for sickle cell disease treatment, conducted by the Foundation for Sickle Cell Disease Research in Florida. Five patients treated over 29 days demonstrated favorable safety and tolerability, with mean pain scores decreasing from 7.0 to 6.6 and directional improvements in red blood cell sickling kinetics and patient-reported outcomes. The company plans to file an Investigational New Drug Application with the FDA later this year to advance toward dose optimization studies.citybizVascarta Appoints Former Johnson & Johnson Executive Richard Serbin as Chief Strategy OfficerVascarta Inc., a clinical-stage biotechnology company, has appointed Richard Serbin as Chief Strategy Officer to support strategic partnerships, evaluate acquisitions, and drive business development as it advances its transdermal drug delivery platform. Serbin brings over 50 years of pharmaceutical and healthcare experience, including senior roles at Johnson & Johnson as Vice President of Corporate Development and previous positions at Schering-Plough and Revlon. The appointment positions Vascarta to navigate regulatory pathways and expand its pipeline targeting sickle cell disease and osteoarthritis.