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NCT03216486WITHDRAWNanonymous

A Phase 2, Non-controlled, Open-Label, Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta

Sponsor

Source record

Ultragenyx Pharmaceutical Inc

Phase

Source record

PHASE2

Modality

AI-normalized

small molecule

Target

AI-normalized

BPS804

Indication / condition

AI-normalized

Osteogenesis Imperfecta

Intervention

Source record

BPS804

Source & freshness

Source record

NCT ID

NCT03216486

Original source

ClinicalTrials.gov

Source last updated

Jul 03, 2023

Ingested at

Jun 11, 2026

Internal sync

Jun 11, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT03216486

Title

A Phase 2, Non-controlled, Open-Label, Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta

Sponsor

Ultragenyx Pharmaceutical Inc

Status

WITHDRAWN

Phase

PHASE2

Condition raw

Osteogenesis Imperfecta

Condition normalized

Osteogenesis Imperfecta

Modality raw

small molecule

Modality normalized

small molecule

Target raw

BPS804

Target normalized

BPS804

Interventions

BPS804

Public preview

Source record

The purpose of this study is to investigate the effect of BPS804 on strength/quality of bone in patients with Type I, III or IV Osteogenesis imperfecta using a special type of CT scanner. Participants will be treated for 1 year.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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TrialSignal

Clinical trial intelligence report

A Phase 2, Non-controlled, Open-Label, Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta

Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.

Generated

Jun 13, 2026

NCT ID

NCT03216486

Status

WITHDRAWN

Phase

PHASE2

Sponsor

Ultragenyx Pharmaceutical Inc

Executive brief

Investment-Ready Snapshot

The purpose of this study is to investigate the effect of BPS804 on strength/quality of bone in patients with Type I, III or IV Osteogenesis imperfecta using a special type of CT scanner. Participants will be treated for 1 year.

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedJul 03, 2023
Internal syncJun 11, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT03216486

Indication

Osteogenesis Imperfecta

Modality

small molecule

Target

BPS804

Intervention

BPS804

Source record

Protocol Description

Detailed source ingestion pending.

Source record

Outcome Measures

Detailed source ingestion pending.

Source record

Eligibility

Detailed source ingestion pending.

AI analysis

Known Results And Readout Context

Detailed source ingestion pending.

IP intelligence

Patent And IP Landscape

Detailed source ingestion pending.

Source record

Contacts

Detailed source ingestion pending.