ClinicalTrials.gg
Enrolling by invitationNCT06873035HCHUpdated Jul 16, 2026

An Interventional Study of Infigratinib in Children With Hypochondroplasia

A Phase 2/3 interventional study of infigratinib 0.128 mg/kg/day and infigratinib 0.25 mg/kg/day in Hypochondroplasia, sponsored by QED Therapeutics, a BridgeBio company. Enrolling by invitation at 24 sites in 10 countries. Open to participants aged 3 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-07-16.

Sponsored by QED Therapeutics, a BridgeBio company (part of BridgeBio) · Phase 2/3, Interventional, and Treatment

Phase
Phase 2/3
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
3 Years to 18 Years
Sex
All
01

Study summary

ACCEL2/3 is a Phase 2/3 study. The purpose of the Phase 2 portion of the study (ACCEL2/3) is to evaluate the efficacy and safety of infigratinib in children with hypochondroplasia (HCH) receiving infigratinib at one of two doses, who have completed at least 26 weeks of participation in QED-sponsored ACCEL (QBGJ398-004).

Read the detailed description

ACCEL 2/3 is a Phase 2/3 study that comprises of 2 portions. The Phase 2 portion is an open-label, portion in children with HCH aged 5 to 11 years old followed by a Phase 3 portion which is double-blind, placebo-controlled in children with HCH aged >3 years old to \<18 years old.

02

Conditions studied

  • Hypochondroplasia

Keywords

  • skeletal dysplasia
  • endochondral ossification
  • hypochondroplasia
  • HCH
  • shortened proximal limbs
  • fibroblast growth factor receptor 3
  • FGFR3
  • endochondral bone formation
  • disproportionate short stature
  • quality of life
  • dwarfism
  • bone diseases
  • musculoskeletal diseases
  • osteochondrodysplasia
  • functional abilities
  • annualized growth velocity
  • annualized height velocity
  • growth
  • genetic diseases
  • congenital
  • AHV
  • AGV
  • Pathogenic variants
03

In context

Mucopolysaccharidosis IV

101 studies on the registry are indexed under Mucopolysaccharidosis IV; 27 are open to participants now.

This study's planned enrollment of 24 is below the median of 61 across 56 interventional studies indexed under Mucopolysaccharidosis IV.

Browse Mucopolysaccharidosis IV studies →

Lead sponsor

QED Therapeutics, a BridgeBio company is the lead sponsor of 8 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  • Participants must have completed at least 26 weeks and still be on the observational study (QBGJ398-004).
  • Phase 2 portion: Participants 5-11 years of age (inclusive).
  • Phase 3 portion: Participants 3 to \<18 years of age at screening with growth potential
  • Diagnosis of HCH documented clinically by the presence of disproportionate short stature and confirmed with a molecular test.
  • Participants are able to swallow oral medication.
  • Participants and parent(s), legal guardian(s), or caregiver(s) are willing and able to comply with study visits and study procedures.
  • Participants are ambulatory and able to stand without assistance. Sex and /Barrier Requirements
  • Negative pregnancy test in girls ≥10 years of age or girls of any age who have experienced menarche.
  • If sexually active, participants whether male or female, must be willing to use a highly effective method of contraception, as relevant, while taking study drug and for 1 month after the last dose of study drug.
  • Signed .

Key Exclusion Criteria:

  • Participants who have ACH or a short stature condition other than HCH.
  • Significant concurrent disease or condition that, in the view of the investigator and/or sponsor, would confound assessment of efficacy or safety of infigratinib.
  • Current evidence of corneal or retinal disorder/keratopathy confirmed by ophthalmic examination.
  • Concurrent circumstance, disease, or condition that, in the view of the investigator and/or sponsor, would interfere with study participation or safety evaluations.
  • History and/or current evidence of extensive ectopic tissue calcification.
  • History of .
  • Having received or planning to receive treatment with any other or approved product for the treatment of ACH, HCH, or short stature.
  • Regular long-term treatment (≥3 weeks) with supraphysiologic doses of .
  • Previous limb-lengthening surgery at any time or planned/expected to have limb-lengthening or guided growth surgery while participating in the study.
  • Participants receiving medications which could increase serum phosphorus and/or calcium concentrations
  • Clinically significant abnormality in any laboratory test result at screening.
  • Pregnant or breastfeeding at the screening visit or planning to become pregnant (self or partner) at any time during the study.
  • Allergy to any components of the study drug.
  • Concurrent circumstance, disease, or condition that would interfere with study participation.
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Phase 2 Cohort 1

    Oral infigratinib 0.128 mg/kg/day

    Drug: infigratinib 0.128 mg/kg/day

  • Experimental
    Phase 2 Cohort 2

    Oral infigratinib 0.25 mg/kg/day

    Drug: infigratinib 0.25 mg/kg/day

Interventions

  • Druginfigratinib 0.128 mg/kg/day

    Drug page: Infigratinib

    Oral infigratinib 0.128 mg/kg/day

  • Druginfigratinib 0.25 mg/kg/day

    Drug page: Infigratinib

    Oral infigratinib 0.25 mg/kg/day

06

What researchers measure

Primary outcomes

  1. Change from baseline (BL) in Annualized Height Velocity (AHV; cm/year)

    Time frame: 26 weeks

  2. Incidence, severity, and seriousness of adverse events (AEs) that require dose reduction or discontinuation

    Time frame: at least 26 weeks

Secondary outcomes

  1. Change from BL in height Z-score (in relation to both HCH and average height tables)

    Time frame: 52 weeks

  2. Change from BL in upper to lower body segment ratio (cm)

    Time frame: 52 weeks

  3. Changes in cognitive function (as assessed by age appropriate computerized tests)

    Time frame: 52 weeks

  4. Pharmacokinetic profile of infigratinib by assessment of maximum concentration (Cmax)

    Time frame: 52 weeks

  5. Pharmacokinetic profile of infigratinib by assessment of time-to-maximum concentration (Tmax)

    Time frame: 52 weeks

  6. Change from BL in collagen X marker (CXM) levels

    Time frame: 52 weeks

Other outcomes

  1. Change from BL in comorbidities associated with HCH

    Time frame: 52 weeks

  2. Change from BL in Health-related Quality of Life (HRQoL) (as assessed by Pediatric Quality of Life Inventory [PedsQL tool])

    Time frame: 52 weeks

  3. Evaluate treatment benefit as assessed by qualitative interviews

    Time frame: 52 weeks

07

Study locations

24 sites
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2025 (actual). Primary completion is estimated for Jan 2027, 21 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 18, 2025
First posted
Mar 12, 2025
StartActual
Apr 22, 2025
Primary completionEst.
Jan 2027
CompletionEst.
Jan 2027
Last update
Jul 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06873035
Responsible party
Sponsor
First posted
Mar 12, 2025
Start date
Apr 22, 2025
Primary completion
Jan 2027 (estimated)
Completion
Jan 2027 (estimated)
Last update
Jul 16, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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