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The data shows that ARU-1801 offers potential long-term improvement of the primary symptoms seen with SCD without the toxicities and resource utilization associated with fully myeloablative chemotherapies.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 10, 2022

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Data demonstrate that ARU-1801 gene therapy may not only be able to reduce severe vaso-occlusive events but also reduce days in hospital for SCD patients, which could provide a clinically meaningful benefit for patients and help reduce health care costs.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 16, 2022

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ARU-1801 is designed to address the limitations of current curative allogeneic transplant options, such as low donor availability, the risk of graft-versus-host disease and toxicity from myeloablative chemotherapy.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 19, 2022

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Under the terms of the agreement, Aldevron will provide good manufacturing practice (GMP)-grade plasmid for Aruvant's upcoming ARU-1801 pivotal trial.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Recipient: Aldevron

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Partnership June 16, 2021

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The agreement aims to support ARU-1801, Aruvant’s one-time investigational gene therapy for sickle cell disease (SCD). Aruvant has chosen Lonza to help develop and manufacture ARU-1801 for its upcoming pivotal trial.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Recipient: Lonza Group

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Partnership January 18, 2021

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Preliminary clinical data from Aruvant's ongoing Phase 1/2 study that demonstrates ARU-1801, administered with only reduced intensity conditioning, can achieve durable reductions in disease burden.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 16, 2020

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Data presented at ASH is from the MOMENTUM study, an open label Phase 1/2 clinical trial examining ARU-1801 as a one-time potentially curative gene therapy for individuals with sickle cell disease (SCD).


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 04, 2020

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In partnership with SCDAA, Aruvant is working to educate patients about gene therapy, while gaining critical insights from the patient community for its ARU-1801 SCD development program.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: ARU-1801

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Sickle Cell Disease Association of America

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Partnership October 12, 2020

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Aruvant's ARU-1801, received FDA Orphan Drug designation for its efficacy to deliver a highly potent gene payload with enhanced anti-sickling properties, for a Reduced Intensity Conditioning regimen.


Lead Product(s): ARU-1801

Therapeutic Area: Genetic Disease Product Name: Undisclosed

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 22, 2020

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