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Respiratory Syncytial Virus Infection

Respiratory
10
Pipeline Programs
9
Companies
15
Clinical Trials
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
3
4
2
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
538%
Small Molecule
431%
Vaccine
323%
RNA Therapeutic
18%
+ 6 programs with unclassified modality

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.

Competitive Landscape

9 companies ranked by most advanced pipeline stage

Abbott
AbbottABBOTT PARK, IL
4 programs
1
1
PalivizumabPhase 3Monoclonal Antibody1 trial
palivizumabPhase 2/3Monoclonal Antibody1 trial
Surveillance of Synagis in Korean Pediatric PatientsN/A1 trial
SynagisN/A1 trial
Active Trials
NCT01537198Completed618Est. Jun 2014
NCT01107535Completed82Est. Feb 2011
NCT01006629Completed100Est. Jul 2010
+1 more trials
AbbVie
AbbVieNORTH CHICAGO, IL
2 programs
1
PalivizumabPhase 3Monoclonal Antibody
Surveillance of Synagis in Korean Pediatric PatientsN/A
Pfizer
PfizerNEW YORK, NY
3 programs
1
1
SisunatovirPhase 2/3Small Molecule1 trial
SisunatovirPhase 1Small Molecule1 trial
RSVpreF vaccineN/AVaccine1 trial
Active Trials
NCT06546800Active Not Recruiting1,100Est. Oct 2027
NCT05987072Completed12Est. Dec 2023
NCT06079320Terminated16Est. Sep 2024
MSD
MSDIreland - Ballydine
1 program
1
ClesrovimabPhase 2/3Monoclonal Antibody
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
ClesrovimabPhase 2/3Monoclonal Antibody1 trial
Active Trials
NCT04767373Completed3,632Est. Jul 2024
Kite Pharma
Kite PharmaCA - El Segundo
2 programs
2
PresatovirPhase 2Small Molecule1 trial
PresatovirPhase 2Small Molecule1 trial
Active Trials
NCT02254421Completed60Est. Apr 2017
NCT02135614Completed189Est. Apr 2017
ADMA Biologics
ADMA BiologicsNJ - Ramsey
1 program
1
Immune Globulin Intravenous (Human)Phase 2
Sanofi
SanofiPARIS, France
4 programs
ALX-0171PHASE_11 trial
RSV/hMPV mRNA LNP 1PHASE_1RNA Therapeutic1 trial
parainfluenza virus type 3 vaccinePHASE_1Vaccine1 trial
RSV/hMPV vaccine candidate Dose LPHASE_1_2Vaccine1 trial
Active Trials
NCT01909843Completed24Est. Dec 2013
NCT06237296Completed558Est. Feb 2025
NCT06604767Completed390Est. Mar 2026
+1 more trials
Vigonvita
VigonvitaChina - Suzhou
1 program
Deuremidevir Hydrobromide for SuspensionPHASE_21 trial
Active Trials
NCT06206720Completed60Est. Jun 2025

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
AbbottPalivizumab
PfizerSisunatovir
Sharp TherapeuticsClesrovimab
Abbottpalivizumab
VigonvitaDeuremidevir Hydrobromide for Suspension
Kite PharmaPresatovir
Kite PharmaPresatovir
SanofiRSV/hMPV vaccine candidate Dose L
Sanofiparainfluenza virus type 3 vaccine
SanofiRSV/hMPV mRNA LNP 1
PfizerSisunatovir
SanofiALX-0171
PfizerRSVpreF vaccine
AbbottSurveillance of Synagis in Korean Pediatric Patients
AbbottSynagis

Clinical Trials (15)

Total enrollment: 7,515 patients across 15 trials

Clinical Study of Palivizumab in Japanese Newborns, Infants and Young Children at the Age of 24 Months or Less With Immunocompromised Medical Conditions

Start: Aug 2011Est. completion: Apr 201228 patients
Phase 3Completed

A Study to Learn About the Study Medicine Sisunatovir in Adults With Respiratory Syncytial Virus (RSV) Infection

Start: Dec 2023Est. completion: Sep 202416 patients
Phase 2/3Terminated

Efficacy and Safety of Clesrovimab (MK-1654) in Infants (MK-1654-004)

Start: Apr 2021Est. completion: Jul 20243,632 patients
Phase 2/3Completed

Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in Russian Children

Start: Nov 2009Est. completion: Jul 2010100 patients
Phase 2/3Completed
NCT06206720VigonvitaDeuremidevir Hydrobromide for Suspension

A Study of Deuremidevir Hydrobromide for Suspension in Chinese Infants Hospitalized With RSV

Start: Jan 2024Est. completion: Jun 202560 patients
Phase 2Completed

Presatovir in Hematopoietic Cell Transplant Recipients With Respiratory Syncytial Virus (RSV) Infection of the Lower Respiratory Tract

Start: Jan 2015Est. completion: Apr 201760 patients
Phase 2Completed

Efficacy, Pharmacokinetics, and Safety of Presatovir in Hospitalized Adults With Respiratory Syncytial Virus (RSV) Infection

Start: Jun 2014Est. completion: Apr 2017189 patients
Phase 2Completed
NCT06134648SanofiRSV/hMPV vaccine candidate Dose L

Study of a Respiratory Syncytial Virus/Human Metapneumovirus Vaccine Candidate

Start: Nov 2023Est. completion: Feb 2026646 patients
Phase 1/2Completed
NCT06604767Sanofiparainfluenza virus type 3 vaccine

Study of a Respiratory Syncytial Virus/Human Metapneumovirus/Parainfluenza Virus Type 3 Vaccine Candidate in Adults Aged 60 Years and Older

Start: Sep 2024Est. completion: Mar 2026390 patients
Phase 1Completed
NCT06237296SanofiRSV/hMPV mRNA LNP 1

Study of the Safety and Immune Response of an Investigational mRNA Vaccine for the Prevention of Respiratory Syncytial Virus and/or Human Metapneumovirus in Participants Aged 18 to 49 Years and 60 Years and Older

Start: Jan 2024Est. completion: Feb 2025558 patients
Phase 1Completed

A Study to Learn How the Study Medicine Called Sisunatovir is Tolerated and Acts in the Bodies of Chinese Healthy Adults.

Start: Nov 2023Est. completion: Dec 202312 patients
Phase 1Completed

ALX-0171 Safety Study in Adults With Hyperresponsive Airways

Start: Jul 2013Est. completion: Dec 201324 patients
Phase 1Completed
NCT06546800PfizerRSVpreF vaccine

SPECIAL INVESTIGATION FOR ABRYSVO IN INDIVIDUALS AGED 60 YEARS OR OLDER

Start: May 2025Est. completion: Oct 20271,100 patients
N/AActive Not Recruiting
NCT01537198AbbottSurveillance of Synagis in Korean Pediatric Patients

Surveillance of Synagis in Korean Pediatric Patients

Start: Jan 2012Est. completion: Jun 2014618 patients
N/ACompleted

Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants With High Risk of Severe Respiratory Syncytial Virus (RSV) Infection

Start: Sep 2007Est. completion: Feb 201182 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

2 late-stage (Phase 3) programs, potential near-term approvals
9 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.