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NCT03799627COMPLETEDanonymous

Phase 2, Randomized, Open-Label, Active-Controlled, Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics Study of Oral Vadadustat for the Treatment of Anemia in Hemodialysis Subjects Converting From Epoetin Alfa (FO2RWARD-2)

Sponsor

Source record

Akebia Therapeutics

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Anemia in Hemodialysis Participants

Indication / condition

AI-normalized

Anemia

Intervention

Source record

Vadadustat, Epoetin Alfa, Vadadustat TIW

Source & freshness

Source record

NCT ID

NCT03799627

Original source

ClinicalTrials.gov

Source last updated

Sep 29, 2022

Ingested at

Jun 03, 2026

Internal sync

Jun 05, 2026

Model version

trialsignal-ai-v1

Normalized confidence

88%

Validation status

validated

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View original source fields

NCT ID

NCT03799627

Title

Phase 2, Randomized, Open-Label, Active-Controlled, Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics Study of Oral Vadadustat for the Treatment of Anemia in Hemodialysis Subjects Converting From Epoetin Alfa (FO2RWARD-2)

Sponsor

Akebia Therapeutics

Status

COMPLETED

Phase

Phase 2

Condition raw

Anemia

Condition normalized

Anemia

Modality raw

Anemia

Modality normalized

small molecule

Target raw

Anemia in Hemodialysis Participants

Target normalized

Anemia in Hemodialysis Participants

Interventions

Vadadustat, Epoetin Alfa, Vadadustat TIW

Public preview

Source record

The clinical trial evaluated Vadadustat, an oral medication, for treating anemia in hemodialysis patients transitioning from Epoetin Alfa. Conducted by Akebia Therapeutics, the study aimed to determine the drug's efficacy, safety, and pharmacokinetics in maintaining hemoglobin levels within a target range.

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

Phase 2, Randomized, Open-Label, Active-Controlled, Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics Study of Oral Vadadustat for the Treatment of Anemia in Hemodialysis Subjects Converting From Epoetin Alfa (FO2RWARD-2)

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

Generated

Jun 13, 2026

NCT ID

NCT03799627

Status

COMPLETED

Phase

Phase 2

Sponsor

Akebia Therapeutics

Executive brief

Investment-Ready Snapshot

The clinical trial evaluated Vadadustat, an oral medication, for treating anemia in hemodialysis patients transitioning from Epoetin Alfa. Conducted by Akebia Therapeutics, the study aimed to determine the drug's efficacy, safety, and pharmacokinetics in maintaining hemoglobin levels within a target range.

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedSep 29, 2022
Internal syncJun 05, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT03799627

Indication

Anemia

Modality

small molecule

Target

Anemia in Hemodialysis Participants

Intervention

Vadadustat, Epoetin Alfa, Vadadustat TIW

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.