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Angion Biomedica
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Country
U.S.A
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Address
456 Montgomery Street, Suite 1200 San Francisco, CA 94104
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Telephone
(415) 655-4899

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The combined company will focus on the advancement of its clinical development program, ELI-002, a therapeutic cancer vaccine designed with Elicio’s proprietary lymph node-targeting AMP technology, being evaluated in patients with mKRAS-driven solid tumors.


Lead Product(s): ELI-002

Therapeutic Area: Oncology Product Name: ELI-002 7P

Highest Development Status: Phase I/ Phase IIProduct Type: Vaccine

Partner/Sponsor/Collaborator: Elicio Therapeutics

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Merger June 01, 2023

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The combined company will focus on advancing Elicio’s proprietary lymph node-targeting Amphiphile (AMP) technology to develop immunotherapies, with a focus on ELI-002, a therapeutic cancer vaccine targeting mKRAS-driven tumors.


Lead Product(s): ELI-002

Therapeutic Area: Oncology Product Name: ELI-002

Highest Development Status: Phase IProduct Type: Vaccine

Recipient: Elicio Therapeutics

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Merger January 17, 2023

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ANG-3070, an oral tyrosine kinase inhibitor (TKI), in patients with primary proteinuric kidney diseases, specifically focal segmental glomerulosclerosis (FSGS) and immunoglobulin A nephropathy (IgAN).


Lead Product(s): ANG-3070

Therapeutic Area: Nephrology Product Name: ANG-3070

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 29, 2022

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ANG-3070 is an oral tyrosine kinase inhibitor targeting platelet-derived growth factor receptor alpha and beta and Discoidin Domain Receptors 1 and 2 (DDR1 and DDR2), tyrosine kinase receptors linked to the development of fibrosis in the kidneys and lungs.


Lead Product(s): ANG-3070

Therapeutic Area: Nephrology Product Name: ANG-3070

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 16, 2022

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The results from the Phase 2 GUARD trial of Angion’s ANG-3777 in patients undergoing cardiac surgery involving cardiopulmonary bypass at risk for developing acute kidney injury.


Lead Product(s): Terevalefim

Therapeutic Area: Trauma (Emergency, Injury, Surgery) Product Name: ANG-3777

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: CSL Vifor

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 09, 2021

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ANG-3777 is a small molecule designed to mimic the biological activity of hepatocyte growth factor (HGF), trial did not meet its primary endpoint of percentage increase in serum creatinine based upon the area under the curve (AUC).


Lead Product(s): Terevalefim

Therapeutic Area: Trauma (Emergency, Injury, Surgery) Product Name: ANG-3777

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 09, 2021

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The presentation describes preclinical data from a study of ANG-3070 in a mouse unilateral ureteral obstruction (UUO) model, a well-established model for obstructive renal disease.


Lead Product(s): ANG-3070

Therapeutic Area: Nephrology Product Name: ANG-3070

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 05, 2021

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The overall safety profile of ANG-3777 in this trial was consistent with the overall experience in its clinical development program and consistent with the published literature in this patient population.


Lead Product(s): Terevalefim

Therapeutic Area: Trauma (Emergency, Injury, Surgery) Product Name: ANG-3777

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: CSL Vifor

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 26, 2021

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The Phase 1 study was a randomized, double-blind, and placebo-controlled study in healthy volunteers conducted in Australia to assess the safety, tolerability, pharmacokinetics, and food effect of ANG-3070 dosed orally.


Lead Product(s): ANG-3070

Therapeutic Area: Nephrology Product Name: ANG-3070

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 03, 2021

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Under the terms of the agreement, Vifor Pharma will receive an exclusive global license, excluding China, Taiwan, Hong Kong and Macau, for all ANG-3777 nephrology indications.


Lead Product(s): Terevalefim

Therapeutic Area: Trauma (Emergency, Injury, Surgery) Product Name: ANG-3777

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: CSL Vifor

Deal Size: $30.0 million Upfront Cash: $30.0 million

Deal Type: Licensing Agreement November 09, 2020

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