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NCT01977573COMPLETEDanonymous

A 24-week, Phase IIB, Randomized, Controlled, Parallel Group, Multi-center Study to Evaluate the Safety and Efficacy of GSK1278863 in Subjects With Anemia Associated With Chronic Kidney Diseases Who Are Not on Dialysis.

Sponsor

Source record

GlaxoSmithKline

Phase

Source record

Phase IIB

Modality

AI-normalized

small molecule

Target

AI-normalized

Anemia associated with Chronic Kidney Disease (CKD)

Indication / condition

AI-normalized

Anaemia

Intervention

Source record

GSK1278863, rhEPO

Source & freshness

Source record

NCT ID

NCT01977573

Original source

ClinicalTrials.gov

Source last updated

Oct 12, 2018

Ingested at

May 30, 2026

Internal sync

Jun 05, 2026

Model version

trialsignal-ai-v1

Normalized confidence

88%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT01977573

Title

A 24-week, Phase IIB, Randomized, Controlled, Parallel Group, Multi-center Study to Evaluate the Safety and Efficacy of GSK1278863 in Subjects With Anemia Associated With Chronic Kidney Diseases Who Are Not on Dialysis.

Sponsor

GlaxoSmithKline

Status

COMPLETED

Phase

Phase IIB

Condition raw

Anaemia

Condition normalized

Anaemia

Modality raw

Anaemia

Modality normalized

small molecule

Target raw

Anemia associated with Chronic Kidney Disease (CKD)

Target normalized

Anemia associated with Chronic Kidney Disease (CKD)

Interventions

GSK1278863, rhEPO

Public preview

Source record

This study evaluated GSK1278863, a prolyl hydroxylase inhibitor, for safety and efficacy in treating anemia in non-dialysis dependent CKD patients. The trial involved 252 participants, with a focus on optimizing dosing for future Phase 3 trials.

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 24-week, Phase IIB, Randomized, Controlled, Parallel Group, Multi-center Study to Evaluate the Safety and Efficacy of GSK1278863 in Subjects With Anemia Associated With Chronic Kidney Diseases Who Are Not on Dialysis.

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

Generated

Jun 13, 2026

NCT ID

NCT01977573

Status

COMPLETED

Phase

Phase IIB

Sponsor

GlaxoSmithKline

Executive brief

Investment-Ready Snapshot

This study evaluated GSK1278863, a prolyl hydroxylase inhibitor, for safety and efficacy in treating anemia in non-dialysis dependent CKD patients. The trial involved 252 participants, with a focus on optimizing dosing for future Phase 3 trials.

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedOct 12, 2018
Internal syncJun 05, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT01977573

Indication

Anaemia

Modality

small molecule

Target

Anemia associated with Chronic Kidney Disease (CKD)

Intervention

GSK1278863, rhEPO

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.