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Matinas BioPharma Reports 2023 Financial Results and Provides a Business Update

Clear registration pathway and FDA agreement on the ORALTO Phase 3 trial for MAT2203 represent critical steps forward and supports partnership discussions Continued success of Compassionate/Expanded.

United statesSan diegoNew jerseyJeromed jabbourMatinas biopharmaJody cainAsia pacificJohns hopkinsWorld health organizationData review committeeVanderbilt university medical centerUniversity of californiaUniversity of michiganMemorial sloan kettering cancer centerCompassionate expanded use access programOncology program

Matinas BioPharma Reports 2023 Financial Results and Provides a Business Update

Matinas BioPharma Reports 2023 Financial Results and Provides a Business Update
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United statesNew jerseySan diegoAsia pacificJohns hopkinsJeromed jabbourJody cainMatinas biopharmaUniversity of californiaGenentech incCorporate developmentUniversity of michiganKey program updatesMatinas biopharma holdings incVanderbilt university medical centerMemorial sloan kettering cancer center

Form 8-K Matinas BioPharma Holdin For: Mar 25

Form 8-K Matinas BioPharma Holdin For: Mar 25
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Matinas BioPharma Successfully Reaches Agreement with FDA for a Single Phase 3 Registration Trial to Support an NDA for MAT2203 for the Treatment of Invasive Aspergillosis

20.02.2024 - ORALTO Phase 3 trial focused on desired initial target indication of early oral step-down treatment of invasive aspergillosis infections in adults who have limited or no treatment options Non-inferiority trial will enroll approximately 216 patients . Seite 1

United statesJeromed jabbourTheresa matkovitsCompassionate expanded use access programDrug administrationExpanded use access programChief development officerChief executive officerMatinas biopharma holdings chartAtinas biopharma holdings kursAtinas biopharma holdings aktie

Matinas Biopharma Successfully Reaches Agreement With FDA For A Single Phase 3 Registration Trial To Support An NDA For MAT2203 For The Treatment Of I

Matinas Biopharma Successfully Reaches Agreement With FDA For A Single Phase 3 Registration Trial To Support An NDA For MAT2203 For The Treatment Of I
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United statesTheresa matkovitsMatinas biopharmaJeromed jabbourJody cainAsia pacificInfectious diseases society of americaWorld health organizationCompassionate expanded use access programDrug administrationData review committeeTreatment optionsExpanded use access programChief development officerChief executive officerData safety monitoring board