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Not yet recruitingNCT07346547REDCUREUpdated Jan 20, 2026

REDCURE Registry for Chronic Kidney Disease (CKD) Anemia

An observational study in CKD Anemia, sponsored by Nabiqasim Industries (Pvt) Ltd. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-20.

Sponsored by Nabiqasim Industries (Pvt) Ltd · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
384
Ages
18 Years and older
Sex
All
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Study summary

A local registry on CKD-associated anemia aims to provide real-world insights into disease burden, treatment patterns, and outcomes at the national level. It helps capture variations in anemia severity with CKD stages, therapeutic practices and their response. It also supports evidence-based decision-making, identifies gaps in care, and informs locally relevant guidelines and policy planning to improve patient outcomes with oral novel therapy i.e. daprodustat

02

Conditions studied

  • CKD Anemia

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Keywords

  • Daprodustat
  • oral HIF PHI
  • CKD anemia
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In context

Anemia

1,810 studies on the registry are indexed under Anemia; 215 are open to participants now.

This study's planned enrollment of 384 is above the median of 270 across 368 observational studies indexed under Anemia.

Browse Anemia studies →

Lead sponsor

Nabiqasim Industries (Pvt) Ltd is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

patients with Chronic Kidney Disease (CKD) anemia requiring anemia treatment

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults ≥ 18 years 2. Diagnosed CKD-associated anemia Chronic Kidney Disease (CKD) diagnosed as per KDIGO criteria, including: CKD stages G3-G5 (based on )

    • Patients on hemodialysis (HD) or peritoneal dialysis (PD)
    • Post-kidney transplant patients with CKD 3. Receiving or initiating Daprodustat therapy (new start or switch therapy) 4. CKD stages 3-5, dialysis patients (HD/PD), or post-transplant with CKD anemia 5. Able and willing to provide

Exclusion criteria

Exclusion Criteria

  1. Acute Kidney Injury (AKI) without underlying chronicity
  2. Hematologic disorders not related to CKD (e.g hemolytic anemia, aplastic anemia)
  3. Refusal or inability to provide consent
  4. Current enrollment in an interventional trial that restricts real-world data collection
  5. \< 3 months, where follow-up is not feasible
  6. Known to Daprodustat as per local prescribing information
Terms in these criteria, in plain language(4)

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.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

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.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
384 participants (estimated)
Target follow-up
3 Months
Patient registry
Yes

Groups and cohorts

  • Daprodustat arm for CKD anemia patients

    Daprodustat arm for CKD anemia patients

    Drug: Daprodustat

Interventions

  • Hypoxia Inducible Factor (HIF) Prolyl Hydroxylase Inhibitor (PHI) drug

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What researchers measure

Primary outcomes

  1. Serum hemoglobin levels

    Hemoglobin response to therapy

    Time frame: 3 months

Secondary outcomes

  1. Frequency of MACE ( Major Adverse Cardiovascular Events)

    MACE events: * Unstable angina requiring hospitalization * Non-fatal MI * Non-fatal stroke * Cardiovascular death * Other adverse events * Hospitalization episodes . Mortality * Optional patient-reported outcomes (fatigue, functional status)

    Time frame: 3 months

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Study locations

No study locations are listed for this record.

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References and documents

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jan 2026; primary completion for Jan 2027, 12 months later.

Of 145 observational studies under Anemia, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 76. This study's planned 12 months is below that.

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

Registered
Jan 8, 2026
First posted
Jan 16, 2026
StartEst.
Jan 30, 2026
Primary completionEst.
Jan 30, 2027
CompletionEst.
May 31, 2027
Last update
Jan 20, 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 Jan 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07346547
Lead sponsor
Nabiqasim Industries (Pvt) Ltd
Responsible party
Sponsor
First posted
Jan 16, 2026
Start date
Jan 30, 2026 (estimated)
Primary completion
Jan 30, 2027 (estimated)
Completion
May 31, 2027 (estimated)
Last update
Jan 20, 2026

Study contacts

Hussain Abidi
Contact
NQmedicalaffairs@gmail.com
+923322583236

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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