Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Andecaliximab clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our USA register that name Andecaliximab as an intervention. Synced 10 Nov 2026
2Current trials
0Recruiting now
1Lead sponsor
1Country register
At a glance

Andecaliximab is named as an intervention in 2 current clinical trials in our USA register. None are recruiting at the moment. The most common phase is Phase 1/2. The lead sponsor is Ashibio Inc. The most-studied condition is Heterotopic Ossification (HO).

Where Andecaliximab is approved

All regulators →
USUnited States (FDA)
No FDA approval of a single-substance product in Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC
  • 1 EU orphan designation, most recently for treatment of fibrodysplasia ossificans progressiva (19 Feb 2024, positive)

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

How Andecaliximab works

All drug targets →
  • Matrix metalloproteinase 9 inhibitor Inhibitor
    Target: MMP9 matrix metallopeptidase 9
    ✓ In ChEMBL and the Guide to Pharmacology
Diseases it has been tested for in clinical trials, by furthest phase
  • Gastric adenocarcinomaPhase 3
  • Gastroesophageal junction adenocarcinomaPhase 3
  • Ulcerative colitisPhase 3
  • Fibrodysplasia ossificans progressivaPhase 2/3
  • Crohn diseasePhase 2
  • Cystic fibrosisPhase 2
  • Rheumatoid arthritisPhase 2
  • Breast cancerPhase 1
  • Chronic obstructive pulmonary diseasePhase 1
  • Colorectal cancerPhase 1
13 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL3833374, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 9510, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Andecaliximab

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Active, closed2100%

Trials by phase

  • Phase 1/2150%
  • Phase 2/3150%
01

Clinical trials of Andecaliximab

2 trials
StudyPhaseStatusLead sponsorRegisters
A Study of Andecaliximab in Participants With Fibrodysplasia Ossificans Progressiva (FOP)
NCT06508021 · Fibrodysplasia Ossificans Progressiva
Phase 2/3 Active, closed Ashibio Inc USA
A Study of Andecaliximab in People With Spinal Cord Injury at Risk for Bone Growth Outside of the Normal Skeleton.
NCT07024407 · Heterotopic Ossification (HO)
Phase 1/2 Active, closed Ashibio Inc USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Andecaliximab

2 conditions
Heterotopic Ossification (HO)1Fibrodysplasia Ossificans Progressiva1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Ashibio Inc2
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA20

A trial with sites in more than one country appears in each of those registers.

05

Questions about Andecaliximab trials

How many clinical trials are testing Andecaliximab?

2 current trials in our USA register name Andecaliximab as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Andecaliximab trials recruiting patients?

Not at the moment. None of the 2 trials in our registers is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Who sponsors Andecaliximab clinical trials?

The lead sponsor is Ashibio Inc. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Andecaliximab works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Andecaliximab works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Andecaliximab (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.