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Autosomal Dominant Polycystic Kidney Disease

Nephrology
10
Pipeline Programs
7
Companies
12
Clinical Trials
2 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
7
0
2
0
Early DiscoveryClinical DevelopmentMarket

Nephrology is a $36.6B mature market dominated by cardiometabolic crossover drugs with limited pure renal innovation.

$36.6B marketMature→ Stable30 products15 companies

Key Trends

  • GLP-1 agonists and SGLT2 inhibitors dominate (69% of spending) due to dual cardio-renal benefits
  • Patent cliffs approaching 2026-2030 create generic conversion risk for blockbuster franchises
  • Pipeline activity remains robust (2,785 trials) but concentrated in early-phase basic research

Career Verdict

Nephrology offers stable employment in commercial and medical affairs roles, but limited growth upside due to mature blockbuster dependency and declining pure renal research focus.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1OZEMPICStable
$9.2B
Novo Nordisk·Peak12.4yr
#2JARDIANCEStable
$8.8B
#4FARXIGAStable
$4.3B
AstraZeneca·Peak15.4yr

Drug Class Breakdown

Glucagon-like Peptide-1 (GLP-1) Agonists
$16.6B(45%)

cardiometabolic dominance

Sodium-Glucose Transporter 2 Inhibitors
$8.8B(24%)

cardioprotective expansion

SGLT2 Inhibitors (dapagliflozin class)
$4.3B(12%)

heart failure crossover

Adrenergic Beta3-Agonists
$3.0B(8%)

overactive bladder niche

Dipeptidyl Peptidase 4 Inhibitors
$1.3B(4%)

declining relevance

Career Outlook

Stable

Nephrology careers are stable but not expanding; the field is supported by blockbuster drugs (GLP-1s, SGLT2i) that face patent cliffs between 2026–2041, creating near-term employment security but long-term uncertainty. Commercial and medical affairs roles dominate hiring, while R&D investment is limited to niche mechanisms (complement inhibition, gene therapy). Career progression depends on specialization in medtech, diagnostics, or orphan nephrology rather than traditional pharma blockbuster development.

Breaking In

Target medtech platforms (Outset, Fresenius) or biotech innovators (Vertex, Calyxo) over traditional pharma; nephrology offers job stability and clinical depth but limited growth trajectory in pure pharmaceutical roles.

For Experienced Professionals

Leverage cardiometabolic expertise to span diabetes, CKD, and HF franchises; position for transition to orphan nephrology (ADPKD, FSGS, IgA) where innovation and valuation multiples are highest.

In-Demand Skills

Renal endpoints and biomarkers (eGFR, albuminuria)Cardio-renal crossover knowledge (diabetes + CKD + HF)Medtech systems expertise (dialysis, transplantation platforms)Medical affairs and key opinion leader management

Best For

Medical Science Liaison (renal specialists)Commercial Manager (established nephro franchise)Clinical Development Manager (rare kidney disease)Real-world evidence analyst (CKD outcomes)

Hiring Landscape

$108K–$330K

Nephrology hiring is concentrated in commercial roles (58 positions, $108K avg) and medical affairs (12 positions, $330K avg), reflecting mature market dynamics. Top hiring companies are innovative platforms (Vertex: 41 jobs) and medtech (Outset: 21 jobs), not traditional pharma. Salary compression in commercial roles suggests commoditization.

124
Open Roles
5
Companies Hiring
4
Departments

Top Hiring Companies

20Growing
8Stable

By Department

Commercial(47%)
$108K
Medical Affairs(10%)
$330K
Clinical Excellence(6%)
$140K
Quality Assurance(4%)
$201K

Hiring favors medtech and biotech platforms over traditional pharma; medical affairs offers premium compensation but limited volume; commercial roles are abundant but underpaid relative to other therapeutic areas.

Competitive Landscape

7 companies ranked by most advanced pipeline stage

Otsuka
OtsukaJapan - Tokushima
8 programs
6
1
OPC-41061Phase 31 trial
OPC-41061Phase 21 trial
PBPhase 21 trial
TolvaptanPhase 21 trial
TolvaptanPhase 21 trial
+3 more programs
Active Trials
NCT02322385Completed80Est. Dec 2016
NCT00841568Completed17Est. Nov 2010
NCT05190744Completed36Est. Dec 2025
+5 more trials
Sandoz
SandozAustria - Kundl
1 program
1
EverolimusPhase 31 trial
Active Trials
NCT02134899Completed3Est. Nov 2017
AbbVie
AbbVieNORTH CHICAGO, IL
1 program
1
ABBV-CLS-628Phase 2
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
AZD1613 - Part APhase 11 trial
Active Trials
NCT07228364Recruiting40Est. Jan 2027
Kyorin Pharmaceutical
1 program
Clinical Implications of DNA Analysis on ADPKDN/A
Calico
CalicoLONG BEACH, CA
1 program
ABBV-CLS-628PHASE_21 trial
Active Trials
NCT06902558Recruiting240Est. Aug 2029
Galapagos
Galapagos2800 MECHELEN, Belgium
1 program
GLPG2737PHASE_21 trial
Active Trials
NCT04578548Terminated66Est. Apr 2023

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
SandozEverolimus
OtsukaOPC-41061
CalicoABBV-CLS-628
OtsukaPB
GalapagosGLPG2737
OtsukaTolvaptan
OtsukaTolvaptan MR
OtsukaTolvaptan
OtsukaTolvaptan MR
OtsukaOPC-41061
AstraZenecaAZD1613 - Part A
OtsukaClinical Implications of DNA Analysis on ADPKD

Clinical Trials (12)

Total enrollment: 747 patients across 12 trials

The Efficacy of Everolimus in Reducing Total Native Kidney Volume in Polycystic Kidney Disease Transplanted Recipients

Start: Oct 2014Est. completion: Nov 20173 patients
Phase 3Completed

A Long-term Administration Study of OPC-41061 in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) (2) [Extension of Study 156-05-002]

Start: Nov 2009Est. completion: Jul 201413 patients
Phase 3Completed
NCT06902558CalicoABBV-CLS-628

A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of ABBV-CLS-628 in Adult Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Start: Jun 2025Est. completion: Aug 2029240 patients
Phase 2Recruiting

Probenecid (PB) to Treat Hereditary Nephrogenic Diabetes Insipidus (NDI), ADPKD Treated With Tolvaptan, and Severely Polyuric Patients With Previous Lithium Administration

Start: Sep 2022Est. completion: Dec 202536 patients
Phase 2Completed

A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Start: Nov 2020Est. completion: Apr 202366 patients
Phase 2Terminated

Tolvaptan-Octreotide LAR Combination in ADPKD

Start: Dec 2018Est. completion: Dec 202120 patients
Phase 2Completed
NCT01451827OtsukaTolvaptan MR

8-Week Study of Tolvaptan Dose Forms in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Start: Oct 2011Est. completion: Jul 2013178 patients
Phase 2Completed

Short-term Renal Hemodynamic Effects of Tolvaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Start: Oct 2010Est. completion: Nov 201129 patients
Phase 2Completed
NCT01210560OtsukaTolvaptan MR

Dose-finding Study of New Tolvaptan Formulation in Subjects With ADPKD

Start: Oct 2010Est. completion: Jun 201125 patients
Phase 2Completed

A Long-term Administration Study of OPC-41061 in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) [Extension of Study 156-04-001]

Start: Apr 2006Est. completion: Nov 201017 patients
Phase 2Completed
NCT07228364AstraZenecaAZD1613 - Part A

Safety, Tolerability and Pharmacokinetics of AZD1613 in Adults With Autosomal Dominant Polycystic Kidney Disease

Start: Nov 2025Est. completion: Jan 202740 patients
Phase 1Recruiting
NCT02322385OtsukaClinical Implications of DNA Analysis on ADPKD

Clinical Implications of DNA Analysis on ADPKD

Start: Jan 2014Est. completion: Dec 201680 patients
N/ACompleted

Related Jobs in Nephrology

Phase Legend

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

Key Insights

2 late-stage (Phase 3) programs, potential near-term approvals
2 actively recruiting trials targeting 747 patients
7 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.