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    Company profile for Vanda Pharmaceuticals

    NEW Drugs in Dev: 13
    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Guizhou Utide Biotechnology Co., Ltd. - Specialized GMP manufacturing for next-generation GLP-1 peptide APIs.

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    About

    Vanda is developing important new medicines to improve the lives of patients. We use new technologies, including genetics and genomics, to inform our drug discovery, our clinical trials, and our commercial positioning of our compounds. We are working to advance the use of novel approaches to deliver these new medicines to patients. Our CEO, Mihael Polymeropoulos, MD, founded Vanda in 2003 in partnership with Care Capital LLC, ...
    Vanda is developing important new medicines to improve the lives of patients. We use new technologies, including genetics and genomics, to inform our drug discovery, our clinical trials, and our commercial positioning of our compounds. We are working to advance the use of novel approaches to deliver these new medicines to patients. Our CEO, Mihael Polymeropoulos, MD, founded Vanda in 2003 in partnership with Care Capital LLC, a prominent biopharmaceuticals-focused investment firm, and Bio*One Capital, an investment arm of the Singapore government with a focus on new biomedical enterprises.

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    CONTACT DETAILS

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    Vanda PharmaceuticalsUnited_States_of_America Flag
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    2200 Pennsylvania Ave NW Suite 300E Washington, DC 20037
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    202-734-3400
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    enquiries@pharmacompass.com
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    NEWS #PharmaBuzz

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    Vanda Secures Long-Awaited FDA Hearing In Jet Lag Approval bid
    Vanda Secures Long-Awaited FDA Hearing In Jet Lag Approval bid

    05 Mar 2026

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/fda-answers-vandas-years-long-call-formal-hearing-sleep-drug-hetlioz-twice-rejected-jet-lag

    FIERCE PHARMA
    05 Mar 2026
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    Vanda Secures Long-Awaited FDA Hearing In Jet Lag Approval Bid
    Vanda Secures Long-Awaited FDA Hearing In Jet Lag Approval Bid

    04 Mar 2026

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/fda-answers-vandas-years-long-call-formal-hearing-sleep-drug-hetlioz-twice-rejected-jet-lag

    FIERCE PHARMA
    04 Mar 2026
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    FDA Grants Landmark Hearing For HETLIOZ In Jet Lag Disorder
    FDA Grants Landmark Hearing For HETLIOZ In Jet Lag Disorder

    03 Mar 2026

    // PR NEWSWIRE

    https://www.prnewswire.com/news-releases/vanda-announces-fda-grants-landmark-hearing-for-hetlioz-in-jet-lag-disorder-the-first-drug-approval-hearing-in-over-40-years-302702448.html

    PR NEWSWIRE
    03 Mar 2026
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    FDA Accepts Vanda's BLA for Imsidolimab in GPP Psoriasis
    FDA Accepts Vanda's BLA for Imsidolimab in GPP Psoriasis

    25 Feb 2026

    // PR NEWSWIRE

    https://www.prnewswire.com/news-releases/vanda-pharmaceuticals-announces-fda-acceptance-of-biologics-license-application-filing-for-imsidolimab-for-the-treatment-of-generalized-pustular-psoriasis-302696991.html

    PR NEWSWIRE
    25 Feb 2026
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    US FDA Approves Vanda's Antipsychotic Pill, Shares Climb
    US FDA Approves Vanda's Antipsychotic Pill, Shares Climb

    23 Feb 2026

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-vandas-psychiatric-drug-2026-02-20/

    REUTERS
    23 Feb 2026
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    Vanda Pharms’ Bysanti Receives Approval in US
    Vanda Pharms’ Bysanti Receives Approval in US

    20 Feb 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=220358

    FDA
    20 Feb 2026
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