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Atopic Asthma

Respiratory
2
Pipeline Programs
5
Companies
50
Clinical Trials
1
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
1
Early DiscoveryClinical DevelopmentMarket

Respiratory is a $39.4B mature market dominated by established inhalers and combination therapies with significant patent cliff risk.

$39.4B marketMature→ Stable30 products15 companies

Key Trends

  • Consolidation around GSK's triple-therapy franchises (Trelegy, Breo, Anoro)
  • Major patent expirations 2026-2031 creating $7.8B revenue cliff
  • High clinical trial activity (4,862 trials) suggesting pipeline innovation despite market maturity

Career Verdict

Respiratory offers stable commercial careers but limited growth upside; best for professionals seeking established markets with strong commercial infrastructure rather than innovation-driven advancement.

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

Market Leaders

#1ELIQUISGrowing
$18.3B
Bristol Myers Squibb·Launch15.0yr
#3TRELEGY ELLIPTADeclining
$4.5B
GSK·Peak4.9yr
#4CREONDeclining
$1.5B
AbbVie·Approaching LOE
#5BREO ELLIPTADeclining
$1.4B
GSK·Peak4.9yr

Drug Class Breakdown

FXa Inhibitors
$18.3B(46%)

dominant market driver

Unknown/Undisclosed Mechanism
$9.7B(25%)

fragmented portfolio

GLP-1 Receptor Agonists
$7.4B(19%)

rapidly expanding

Pancreatic Enzymes
$1.5B(4%)

legacy product

Corticosteroid/LABA Combinations
$796M(2%)

patent cliff approaching

Long-Acting Muscarinic Antagonists
$456M(1%)

mature maintenance therapy

Career Outlook

Stable

Respiratory is a stable, mature market suitable for commercial and medical affairs professionals seeking established career paths, but offers limited growth or innovation-focused opportunities. The impending patent cliff ($7.8B+ revenue at risk 2026-2031) will drive near-term restructuring and consolidation, potentially reducing headcount in 2027-2028. Professionals should expect strong compensation in Medical Affairs and field roles but limited advancement into strategic or R&D positions.

Breaking In

New graduates should prioritize commercial, field-based, or Medical Affairs roles over R&D; respiratory offers structured training and stable compensation but limited innovation exposure, so pair this experience with cross-therapeutic skill-building for long-term mobility.

For Experienced Professionals

Experienced professionals should evaluate whether to maximize earnings in this mature, stable market or transition to higher-growth areas (oncology, cell therapy); respiratory consolidation 2027-2030 will reduce senior-level opportunities, so consider strategic moves before patent cliff impacts headcount.

In-Demand Skills

Commercial execution and territory managementMedical Affairs/Key Opinion Leader engagementRegulatory affairs and lifecycle managementInhalation device expertise and product trainingManaged care and payer negotiations

Best For

Brand ManagerMedical Science LiaisonRegional Sales ManagerField Medical RepresentativePayer Relations ManagerRegulatory Specialist

Hiring Landscape

$84K-$314K

The respiratory sector shows modest hiring momentum (510 jobs across tracked positions) concentrated in commercial and engineering roles, with AstraZeneca and GSK leading. Medical Affairs positions command premium salaries ($314K avg) but represent only 3% of openings, reflecting the mature market's focus on sales execution over innovation. Hiring velocity is moderate and reflects market consolidation rather than expansion, suggesting limited career progression opportunities for early-to-mid career professionals.

510
Open Roles
5
Companies Hiring
5
Departments

Top Hiring Companies

43Stable
70Growing
45Stable
15Stable

By Department

Commercial(23%)
$122K
Engineering(11%)
$111K
Medical Affairs(3%)
$314K
IT(4%)
$84K
Manufacturing(3%)

Respiratory hiring favors commercial and field-based roles over R&D; Medical Affairs roles offer premium compensation but are scarce, making this area competitive for specialized talent.

On Market (1)

Approved therapies currently available

Bristol Myers Squibb
ORENCIAApproved
abatacept
Bristol Myers Squibb
Selective T Cell Costimulation Modulator [EPC]iv (infusion)2005
54M Part D

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Bristol Myers Squibb
1 program
1
ORENCIA(abatacept)PHASE_25 trials
Active Trials
NCT05170672No Longer Available
NCT05981976Completed174Est. Dec 2023
NCT04477642Withdrawn0Est. Dec 2020
+2 more trials
Aldeyra Therapeutics
Aldeyra TherapeuticsMA - Lexington
1 program
1
ADX-629Phase 21 trial
Active Trials
NCT04728711Completed8Est. Jan 2022
Genentech
GenentechCA - Oceanside
1 program
Bone Marrow AspirationN/A1 trial
Active Trials
NCT01420003Completed12Est. Jul 2014

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Bristol Myers Squibbabatacept
Aldeyra TherapeuticsADX-629

Showing 15 of 49 trials with date data

Clinical Trials (50)

Total enrollment: 47,167 patients across 50 trials

Effects of Abatacept on Myocarditis in Rheumatoid Arthritis

Start: Jul 2019Est. completion: Sep 202111 patients
Phase 4Terminated

Rheumatoid Arthritis Memory B Cells and Abatacept

Start: Jun 2019Est. completion: Sep 202125 patients
Phase 4Completed

A Study to Evaluate Biomarkers to Predict Efficacy of Abatacept in Rheumatoid Arthritis

Start: May 2019Est. completion: Jun 202325 patients
Phase 4Completed

Introducing a Single IV Abatacept Treatment in RA Patients Currently Receiving Weekly SC Abatacept to Simulate a Holiday

Start: May 2013Est. completion: Jan 201549 patients
Phase 4Completed

Efficacy and Safety of Abatacept in Patients With Primary Sjögren's Syndrome

Start: Aug 2014Est. completion: Aug 201980 patients
Phase 3Completed

Benefits of Injectable Abatacept Using Magnetic Resonance Imaging (MRI) in Rheumatoid Arthritis (RA) Patients

Start: Jun 2011Est. completion: Apr 201434 patients
Phase 3Completed

Abatacept Versus Adalimumab Head-to-Head

Start: Oct 2009Est. completion: Nov 2012869 patients
Phase 3Completed

Phase IIIB Switching From Intravenous to Subcutaneous Study

Start: May 2008Est. completion: Jan 2012123 patients
Phase 3Completed

Substudy - Low Dose of Abatacept in Subjects With Rheumatoid Arthritis

Start: Apr 2007Est. completion: Oct 2009108 patients
Phase 3Completed

A Phase III Study of Abatacept in Japanese Subjects With Rheumatoid Arthritis

Start: Dec 2006Est. completion: Dec 2010217 patients
Phase 3Completed

Study of Abatacept (BMS-188667) in Subjects With Active Rheumatoid Arthritis on Background Non-biologic DMARDS (Disease Modifying Antirheumatic Drugs) Who Have an Inadequate Response to Anti-TNF Therapy

Start: Apr 2005Est. completion: Aug 20091,286 patients
Phase 3Completed

Impact of Subcutaneous Abatacept in Rheumatoid Arthritis Assessing Inhibition of Structural Damage

Start: Mar 2011Est. completion: Jan 201412 patients
Phase 2/3Completed

Efficacy, Pharmacokinetics, Safety, and Immunogenicity Study of Abatacept Administered Subcutaneously to Treat Rheumatoid Arthritis in Japanese Patients

Start: Dec 2009Est. completion: Oct 2012118 patients
Phase 2/3Completed

Efficacy and Safety Study of Abatacept to Treat Lupus Nephritis

Start: Jun 2007Est. completion: Aug 2011423 patients
Phase 2/3Terminated

A Double Masked, Placebo Controlled, Single Center, Randomized Clinical Trial to Assess the Safety and Efficacy of Subjects With Mild Asthma Induced by the Bronchial Allergen Challenge (BAC)

Start: Jan 2021Est. completion: Jan 20228 patients
Phase 2Completed

Acute GVHD Suppression Using Costimulation Blockade to Expand Non-malignant Transplant

Start: Aug 2019Est. completion: Mar 202730 patients
Phase 2Active Not Recruiting

Pilot Study to Evaluate the Safety and Efficacy of Abatacept in Adults and Children 6 Years and Older With Excessive Loss of Protein in the Urine Due to Either Focal Segmental Glomerulosclerosis (FSGS) or Minimal Change Disease (MCD)

Start: Mar 2016Est. completion: Jan 202036 patients
Phase 2Completed

Abatacept for Patients With Inflammatory Arthritis Associated With Sjögren's Syndrome: an Open-Label Phase II Study

Start: Nov 2013Est. completion: Oct 20140
Phase 2Withdrawn

An Open-Label Single-Arm Clinical Trial to Evaluate The Efficacy of Abatacept in Moderate to Severe Patch Type Alopecia Areata

Start: Sep 2013Est. completion: Jul 201715 patients
Phase 2Completed

The Effect of Inhibition of B7-mediated Costimulation on Allergic Airway Inflammation in Mild Atopic Asthmatics

Start: Oct 2008Est. completion: Feb 201224 patients
Phase 2Completed

Safety Study of Abatacept to Treat Refractory Sarcoidosis

Start: Aug 2008Est. completion: Dec 20081 patients
Phase 2Terminated

Pilot Open Label Clinical Trial With Abatacept in Ankylosing Spondylitis

Start: Jan 2008Est. completion: Dec 200930 patients
Phase 2Unknown

Abatacept in ANCA Associated Vasculitis

Start: Nov 2007Est. completion: Nov 20087 patients
Phase 2Terminated

The Study of Abatacept in Combination With Etanercept

Start: Oct 2000Est. completion: Feb 2007141 patients
Phase 2Completed

Abatacept for Patients With COVID-19 and Respiratory Distress

Start: Aug 2020Est. completion: Dec 20200
Phase 1/2Withdrawn

Safety and Efficacy of Abatacept in Subjects With Chronic Urticaria Who Have Had an Inadequate Response to Anti-histamine Therapy

Start: May 2009Est. completion: Mar 20134 patients
Phase 1/2Completed

A Study to Evaluate the Drug Levels of Abatacept Converted From Drug Substance by Two Different Processes in Healthy Participants

Start: Aug 2023Est. completion: Dec 2023174 patients
Phase 1Completed

A Study to Evaluate the Pharmacokinetics of Abatacept Converted From Drug Substance by Two Different Processes

Start: Nov 2018Est. completion: Apr 2019140 patients
Phase 1Completed

Trial of Orencia in Patients With Myasthenia Gravis

Start: Apr 2017Est. completion: Jul 20196 patients
Phase 1Terminated

Open-label Pilot Study of Abatacept for the Treatment of Vitiligo

Start: Jan 2015Est. completion: May 201810 patients
Phase 1Unknown

Abatacept to Treat Steroid Refractory Chronic Graft Versus Host Disease (cGVHD)

Start: Mar 2014Est. completion: Jan 202456 patients
Phase 1Completed

Study to Characterize the Pharmacokinetics of a Single Dose of SC Abatacept 125 mg Using the BD Autoinjector or the Prefilled Syringe

Start: Jul 2013Est. completion: Nov 2014356 patients
Phase 1Completed

A Pilot Study of the Safety and Efficacy of Abatacept Injections in the Treatment of Behcet's Syndrome

Start: Jun 2012Est. completion: Dec 20183 patients
Phase 1Completed

Study on the Safety of Abatacept in Relapsing Polychondritis

Start: Jan 2011Est. completion: May 20124 patients
Phase 1Completed

Pharmacokinetic Study to Compare the Blood Levels of Low vs High Metal Manufacture of Abatacept

Start: Oct 2010Est. completion: Feb 20110
Phase 1Withdrawn

Vaccination Study of Abatacept (BMS-188667) for Normal Healthy Volunteers

Start: Aug 2004Est. completion: Jan 200580 patients
Phase 1Completed

An Exploratory Study of Changes in Synovial Immune Responses Following BMS-188667 Therapy in Subjects With Active Rheumatoid Arthritis on Background DMARDs Who Have Failed Anti-TNF Therapy

Start: Oct 2003Est. completion: Apr 200516 patients
Phase 1Completed

Comparability DE vs CD-CHO1

Start: Sep 2002Est. completion: Dec 200230 patients
Phase 1Completed

A Study to Assess the Pharmacokinetics, Immunogenicity and Safety of Escalating Doses of BMS-188667 Given as a Single Intravenous Infusion to Patients With Psoriasis Vulgaris

Start: Nov 1995Est. completion: Jun 199632 patients
Phase 1Completed

Phase I Study of BMS-188667 (CTLA4Ig) in Patients With Psoriasis Vulgaris

Start: Aug 1995Est. completion: May 199745 patients
Phase 1Completed

Expanded Access for Abatacept

N/ANo Longer Available

A Post-marketing Study on the Safety of Abatacept Treatment in Denmark Using the Danish Database

Start: Jun 2019Est. completion: Oct 202538,396 patients
N/ACompleted

Safety and Effectiveness of Abatacept in Psoriatic Arthritis Participants

Start: Mar 2018Est. completion: Mar 2022190 patients
N/ACompleted

Impact of Anti-citrullinated Protein Antibody Status on Treatment Response and Treatment Persistence in Participants With Rheumatoid Arthritis (RA) Who Are Treated With Abatacept or Tumor Necrosis Factor Inhibitors in Australia

Start: Oct 2017Est. completion: Dec 20192,052 patients
N/ACompleted

A Study to Determine the Risk of Cancer in Rheumatoid Arthritis (RA) Patients Who Use Abatacept and Other Biologic Agents

Start: Feb 2017Est. completion: Mar 20191,132 patients
N/ACompleted

Assessment of the Effectiveness of IV and SC Abatacept (Orencia) Patient Alert Cards in Patients With Rheumatoid Arthritis in a Sample of EU Countries

Start: Nov 2016Est. completion: Apr 2017203 patients
N/ACompleted

Impact and Use of Abatacept IV for Rheumatoid Arthritis in Real Life Setting

Start: Sep 2016Est. completion: Jan 2018153 patients
N/ACompleted

A Study of Juvenile Idiopathic Arthritis Patients Given Abatacept and the Number of Infections or Malignancies That Occur

Start: Jul 2016Est. completion: Sep 2016264 patients
N/ACompleted

Vaccination Against Pneumococcal in Naïve Abatacept Rheumatoid Arthritis Patients

Start: Mar 2016Est. completion: Jan 202180 patients
N/ACompleted

Patient-Reported Efficacy of Subcutaneous (SC) Abatacept in Rheumatoid Arthritis (RA) - South Africa

Start: Jul 2015Est. completion: Jan 201669 patients
N/ACompleted

Related Jobs in Respiratory

Phase Legend

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

Key Insights

5 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.