AISA Pharma Receives FDA Orphan Drug Designation for AISA-021 for Treatment of Systemic Sclerosis

Company also provides updates on its Phase 2 RECONNOITER Study in Raynaud’s Phenomenon and Systemic Sclerosis and other corporate activities BOSTON, Sept. 9, 2024 /PRNewswire/ — Aisa Pharma, Inc. a private, clinical-stage biopharmaceutical company announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation to AISA-021(cilnidipine), a fourth-generation calcium channel antagonist. […]

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AISA Pharma Announces Start of Phase 2b AISA-021 Study for Raynaud’s Phenomenon in Systemic Sclerosis (SSc)

Phase 2 Data at EULAR AISA-021 Treatment Might Influence Systemic Sclerosis (SSc) Disease Severity BOSTON, June 21, 2023 /PRNewswire/ — Aisa Pharma, Inc. a private, clinical-stage biopharmaceutical company today announced initiation of Part 2 of the RECONNOITER Phase 2 study, evaluating AISA-021, a once-daily novel, oral calcium-channel antagonist (CCB) in patients with SSc and Raynaud’s phenomenon(SSc-RP). The study is

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AISA Pharma Announces NIH-NINDS Award to investigate AISA-021 as a non-opioid analgesic for acute and chronic pain

April 3, 2023 – Boston, MA : Aisa Pharma, Inc. a private, clinical-stage biopharmaceutical company, announces that the National Institute of Neurological Disorders and Stroke (NINDS)- National Institutes of Health (NIH) have awarded the Preclinical Screening Pain Platform (PSPP) award to Aisa’s AISA-021 (cilnidipine), a once-daily novel, investigational, oral calcium-channel antagonist. The PSPP was created

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AISA Pharma Announces Upcoming AISA-021 Data Presentations at AAN and EULAR

AISA-021 impact on key Nav 1.7 pain channel to be presented at AANInitial Positive Phase 2 data from RECONNOITER-1 Trial in Systemic Sclerosis patients with Raynaud’s Phenomenon to be presented at EULAR April 3, 2023 – Boston, MA : Aisa Pharma, Inc. a private, clinical-stage biopharmaceutical company, today announced it will present data on its

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AISA Pharma Announces Positive Data Safety Monitoring Board Review of First Phase 2 Data of AISA-021 to treat Raynaud’s Disease in Scleroderma Patients

Company to Move Forward with Key U.S. Regulatory Applications – Investigational New Drug and Orphan Drug Designation BOSTON, July 26, 2022 — Aisa Pharma, Inc. a privately-funded, clinical-stage biopharmaceutical company, today announced that the Data Safety Monitoring Board (DSMB) for the RECONNOITER Phase 2 study of Aisa’s AISA-021 once-daily novel, oral calcium-channel antagonist has met

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Aisa Pharma Starts Phase 2 Study of its proprietary drug for Raynauds and Scleroderma

AISA Pharma Announces Initiation of Patient Enrollment in Phase 2 Trial of Novel Therapy for Raynaud’s Disease in Scleroderma June 16, 2021 – Boston, MA : Aisa Pharma, Inc. a privately-funded, clinical-stage biopharmaceutical company, announces that it has begun enrolling patients in a Phase 2 study evaluating the novel investigational therapy AISA-021 in patients with

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