BBT-877 Shows Strong Ability to Ease Lung Fibrosis, Early Study Shows

BBT-877 Shows Strong Ability to Ease Lung Fibrosis, Early Study Shows

The idiopathic pulmonary fibrosis (IPF) treatment candidate BBT-877 eased lung fibrosis (scarring) in a mouse model, according to South Korea-based Bridge Biotherapeutics. The company believes that BBT-877 may become the “best-in-class” medication for IPF.

Data from a preclinical study on BBT-877 was presented at the 2nd Annual IPF Summit, Aug. 20-22 in San Francisco.

Bridge’s results in the bleomycin-induced mouse model of IPF demonstrated that, compared to other compounds, BBT-877 was superior in reducing lung fibrosis, as assessed by the Ashcroft score (a common measure to determine the severity of PF) and the deposition of collagen  — a key event in the development of fibrosis.

“It is a great opportunity for Bridge Biotherapeutics to present the outstanding preclinical study results on BBT-877 at the IPF Summit 2018,” James Lee, Bridge’s CEO, said in a press release. Lee said the company “aims to develop BBT-877 as the best-in-class drug for IPF as fast as possible to bring this investigational compound to patients as new treatment option.”

Connect with other patients and share tips on how to manage PF in our online forums!

BBT-877 inhibits the enzyme autotaxin (ATX), regarded as a promising target for diseases including fibrosis and cancer.

ATX plays an important role in the generation of the lipid (fat) cellular signaling molecule lysophosphatidic acid (LPA). Prior studies showed that LPA accelerates lung, kidney, and liver fibrosis by regulating cell proliferation and migration, as well as the release of inflammatory molecules and reduction of apoptosis, which refers to “programmed” cell death, as opposed to cell death caused by injury.

The company plans to start a clinical trial in the United States this year. It also expects to submit an investigational new drug application of BBT-877 to the U.S. Food and Drug Administration (FDA) by the end of the year.

BBT-877 was initially discovered by the Korean biotech company LegoChem Biosciences, which licensed exclusive worldwide rights to Bridge.

GLPG1690, an ATX inhibitor being developed by Belgium-based Galapagos, has been approved to proceed to phase 3 stage. Results showed it prevented lung function decline in the Phase 2 FLORA trial (NCT02738801) in 23 patients with IPF. The Phase 3 program, called ISABELA, intends to support both new drug application (NDA) and Market Authorization Application (MAA) filings in the United States and European Union, respectively.

Besides BBT-877, Bridge is also developing BBT-401, an inhibitor of the protein pellino-1 for the treatment of ulcerative colitis. Among other roles, pellino-1 is implicated in inflammation. A Phase 1 clinical trial (NCT03482648), testing the safety and tolerability of single and multiple ascending oral doses of BBT-401 in healthy volunteers, is enrolling participants in Nebraska.

17 comments

    • Joengbin Ahn says:

      Dear Sharon,

      As the article says, now we are planning to submit a US IND of BBT-877 by the end of this year and a phase 2 clinical study is expected to begin within the next year. Please let us know your contact points with an email address if you would like to get updated with the clinical studies in the US.

      Appreciate your comment!

      Joengbin
      Communications Manager from Bridge Biotherapeutics
      [email protected]

      • Bill Mueller says:

        I have been an IPF patient since 2010 and am interested in your updates and would like to participate in any clinical studies in the U.S.

      • Steven Dragoo says:

        Hi Joengbin,

        I would be interested in your clinical trials USA when you start for BBT-877. Sending you an email to your address you have listed.

        Thanks for sharing this…

        SteveD

    • Joengbin Ahn says:

      Dear Ray,
      Please let us know your contact points with an email address if you would like to get updated with the clinical studies in the US. It is expected to begin within the next year.

      Appreciate your comment!

      Joengbin
      Communications Manager from Bridge Biotherapeutics
      [email protected]

    • Joengbin Ahn says:

      Dear Ray,
      Please let me know your contact points with an email address so that I can help you get updated with the clinical studies in the US. Now we are planning to submit a US IND of BBT-877 by the end of this year and a phase 2 clinical study is expected to begin within the next year.

      Appreciate your comment!

      Joengbin
      Communications Manager from Bridge Biotherapeutics
      [email protected]

  1. Joengbin Ahn says:

    Dear Sharon,

    As the article says, now we are planning to submit a US IND of BBT-877 by the end of this year and a phase 2 clinical study is expected to begin within the next year. Please let us know your contact point with an email address if you would like to get updated with the clinical studies in the US.

    Appreciate your comment!

    Joengbin
    Communications Manager from Bridge Biotherapeutics
    [email protected]

  2. May Mya Win says:

    This is something I look forward to. May I be informed of the progress Of BBT-877.
    Please I pray for quick results as I have been diagnosed as having PF for one year already

Leave a Comment

Your email address will not be published. Required fields are marked *