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Albuminuria

3
Pipeline Programs
3
Companies
3
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
1
0
0
2
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
1100%
+ 2 programs with unclassified modality

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Colorado Therapeutics
Colorado TherapeuticsCO - Louisville
1 program
1
MontelukastPhase 41 trial
Active Trials
NCT05498116Recruiting50Est. Oct 2025
Sandoz
SandozAustria - Kundl
1 program
1
amlodipine/benazeprilPhase 4Small Molecule1 trial
Active Trials
NCT00136773Completed332Est. Nov 2005
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
Dapagliflozin 10Mg TabPhase 21 trial
Active Trials
NCT05268926Terminated9Est. Feb 2023

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Colorado TherapeuticsMontelukast
Sandozamlodipine/benazepril
AstraZenecaDapagliflozin 10Mg Tab

Clinical Trials (3)

Total enrollment: 391 patients across 3 trials

Effect of Montelukast on Kidney and Vascular Function in Type 1 Diabetes

Start: Jan 2023Est. completion: Oct 202550 patients
Phase 4Recruiting
NCT00136773Sandozamlodipine/benazepril

Effects of Amlodipine/Benazepril on Albuminuria in Hypertensive Patients With Type 2 Diabetes Mellitus

Start: Apr 2003Est. completion: Nov 2005332 patients
Phase 4Completed
NCT05268926AstraZenecaDapagliflozin 10Mg Tab

TreatIng Microalbuminuria Over 24 Weeks in Subjects With or Without Type 2 Diabetes or HYpertension

Start: Feb 2022Est. completion: Feb 20239 patients
Phase 2Terminated

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

1 actively recruiting trials targeting 391 patients
3 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.