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Stage IV Non-small Cell Lung Cancer

Oncology
12
Pipeline Programs
9
Companies
9
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
5
5
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
6100%
+ 7 programs with unclassified modality

Oncology is a $53.9B market in consolidation, dominated by a handful of megacap players with blockbuster franchises approaching patent expiration.

$53.9B marketConsolidating→ Stable30 products15 companies

Key Trends

  • Heavy patent cliff exposure (REVLIMID $3.9B LOE 2028, JAKAFI $1.9B LOE 2028)
  • Kinase inhibitors and immunomodulatory agents dominate spend; limited diversification in top 10
  • Clinical trial volume remains exceptionally high (29,145 trials) but concentration in Phase 1-2 signals early-stage pipeline challenges

Career Verdict

Strong near-term opportunity for R&D and medical affairs roles, but competitive landscape and patent cliff urgency favor specialists over generalists.

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

Market Leaders

#1ELIQUISStable
$18.3B
Bristol Myers Squibb·Launch15.0yr
#2FARXIGAStable
$4.3B
AstraZeneca·Peak15.4yr
#3REVLIMIDDeclining
$3.9B
Bristol Myers Squibb·LOE Approaching1.8yr
#4XTANDIStable
$2.6B
Astellas·Peak10.7yr
#5IMBRUVICAStable
$2.4B
AbbVie·Peak8.9yr

Drug Class Breakdown

FXa Inhibitors
$18.3B(34%)

concentrated in single product

SGLT2 Inhibitors
$4.3B(8%)

single dominant product

Kinase Inhibitors
$4.0B(7%)

multi-product class, competitive

Immunomodulatory Agents (Cereblon)
$3.9B(7%)

facing near-term patent cliff

Androgen Receptor Antagonists
$2.6B(5%)

prostate cancer specialty

Protein Kinase Inhibitors
$2.4B(4%)

niche hematologic oncology

JAK Inhibitors
$1.9B(4%)

near-term LOE exposure

Career Outlook

Stable

Oncology remains a premium therapeutic area but faces structural headwinds: top 10 products account for >80% of spend, patent cliffs loom (REVLIMID 2028), and late-stage pipeline thinness suggests slower near-term growth. However, high trial volume and consolidation create demand for specialized expertise in regulatory, clinical operations, and lifecycle management. Pharma professionals with kinase inhibitor, immunomodulatory, or ADC experience are in highest demand.

Breaking In

Entry-level candidates should target CROs (Thermo Fisher, IQVIA), emerging biotech (BeiGene, BeOne), or contract manufacturing; oncology specialization requires demonstrated domain knowledge.

For Experienced Professionals

Experienced professionals should focus on lifecycle/patent strategy roles (high salary, low headcount) or pivot to emerging modalities (ADCs, bispecifics) to avoid commoditization in crowded kinase inhibitor space.

In-Demand Skills

Regulatory strategy & PDUFA navigationKinase inhibitor development (small molecule)Clinical trial operations & site managementLifecycle management & patent strategyMedical affairs (oncology-specific science)Manufacturing scale-up (small molecule & biotech)

Best For

Regulatory Affairs ManagerClinical Operations ManagerMedical Science Liaison (MSL) — OncologyLifecycle ManagerR&D Scientist (medicinal chemistry, ADME)Manufacturing Engineer

Hiring Landscape

$102K–$266K

Oncology hiring is actively concentrated at Thermo Fisher Scientific (CRO/CDMO services, 559 jobs), AstraZeneca (208 jobs), and emerging biotech players like BeiGene (185 jobs). Commercial roles dominate (412 jobs, $136K avg) but R&D positions offer the highest salary premium ($199K avg, 347 roles). Patent cliff urgency is creating acute demand for regulatory, CMC, and lifecycle management expertise.

1,946
Open Roles
5
Companies Hiring
5
Departments

Top Hiring Companies

208Stable
185Growing
167Growing
147Growing

By Department

Commercial(21%)
$136K
Research & Development(18%)
$199K
Clinical Operations(5%)
$181K
Medical Affairs(4%)
$266K
Manufacturing(5%)
$102K

Strong near-term hiring momentum, especially in CRO/CDMO and emerging biotech; Medical Affairs offers highest compensation but limited headcount.

Competitive Landscape

8 companies ranked by most advanced pipeline stage

Prevail Therapeutics
3 programs
1
1
1
RamucirumabPhase 2Monoclonal Antibody1 trial
Cetuximab in combination with Carboplatin/GemcitabinePhase 1/21 trial
NecitumumabPhase 1Monoclonal Antibody1 trial
Active Trials
NCT02451930Completed71Est. Sep 2019
NCT01004731Completed7Est. Jan 2006
NCT02831491Withdrawn0Est. Jan 2018
UNION therapeutics
UNION therapeuticsDenmark - Hellerup
1 program
1
SBRT+TKIPhase 21 trial
Active Trials
NCT03595644Completed74Est. Dec 2020
MSD
MSDIreland - Ballydine
3 programs
1
1
PembrolizumabPhase 1/2Monoclonal Antibody1 trial
NecitumumabPhase 1Monoclonal Antibody
None - Common practiceN/A1 trial
Active Trials
NCT03959137Completed215Est. Oct 2019
NCT03559049Terminated25Est. May 2025
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
2 programs
1
1
PembrolizumabPhase 1/2Monoclonal Antibody
NecitumumabPhase 1Monoclonal Antibody
Valerio Therapeutics
Valerio TherapeuticsFrance - Paris
1 program
1
Belinostat, Carboplatin, PaclitaxelPhase 1/2
SOTIO Biotech
SOTIO BiotechCzech Republic - Prague
1 program
1
DCVAC add on to SOCPhase 1/21 trial
Active Trials
NCT02470468Completed105Est. Nov 2021
Incyte
IncyteDE - Wilmington
1 program
1
Identify any dose-limiting toxicityPhase 11 trial
Active Trials
NCT04906746Active Not Recruiting10Est. Dec 2025
Immunicom
ImmunicomCA - San Diego
1 program
1
ImmunicomAIACPhase 11 trial
Active Trials
NCT04142931Unknown30Est. Dec 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
UNION therapeuticsSBRT+TKI
Prevail TherapeuticsRamucirumab
MSDPembrolizumab
SOTIO BiotechDCVAC add on to SOC
Prevail TherapeuticsCetuximab in combination with Carboplatin/Gemcitabine
IncyteIdentify any dose-limiting toxicity
ImmunicomImmunicomAIAC
Prevail TherapeuticsNecitumumab
MSDNone - Common practice

Clinical Trials (9)

Total enrollment: 537 patients across 9 trials

Maintenance Targeted Therapy With or Without Stereotactic Body Radiation Therapy for Stage IV Non-small Cell Lung Cancer

Start: Feb 2017Est. completion: Dec 202074 patients
Phase 2Completed

A Study of Ramucirumab (LY3009806) in Combination With Weekly Docetaxel in Participants With Stage IV Non-Small Cell Lung Cancer

Start: Nov 2016Est. completion: Jan 20180
Phase 2Withdrawn
NCT03559049MSDPembrolizumab

Rucaparib and Pembrolizumab for Maintenance Therapy in Stage IV Non-Squamous Non-Small Cell Lung Cancer

Start: Dec 2018Est. completion: May 202525 patients
Phase 1/2Terminated
NCT02470468SOTIO BiotechDCVAC add on to SOC

Evaluation of Safety and Efficacy of DCVAC/LuCa (Immunotherapy of Lung Cancer) in Patients With Metastatic Lung Cancer

Start: Dec 2014Est. completion: Nov 2021105 patients
Phase 1/2Completed
NCT01004731Prevail TherapeuticsCetuximab in combination with Carboplatin/Gemcitabine

Study of Anti-Epidermal Growth Factor Receptor (EGFr) Antibody, Cetuximab, in Combination With Gemcitabine/Carboplatin in Patients With Stage IV Lung Cancer

Start: Jun 2001Est. completion: Jan 20067 patients
Phase 1/2Completed
NCT04906746IncyteIdentify any dose-limiting toxicity

Ruxolitinib for Cancer Cachexia

Start: Feb 2022Est. completion: Dec 202510 patients
Phase 1Active Not Recruiting

Sequentional Immuno Apheresis Plasma Volume Escalation Cohort Study of Reduction of Soluble Tumor Necrosis Factor Receptors 1 and 2 (sTNFR1/2) With or Without Nivolumab in Patients With Inoperable or Metastatic Solid Tumors

Start: Feb 2020Est. completion: Dec 202230 patients
Phase 1Unknown

A Study of the Combination of Necitumumab (LY3012211) and Pembrolizumab (MK3475) in Participants With NSCLC

Start: Sep 2015Est. completion: Sep 201971 patients
Phase 1Completed
NCT03959137MSDNone - Common practice

BEPACT- Lung: Impact of Patient Characteristics on Pneumo-oncologists Non Small Cell Lung Cancer (NSCLC) Systemic Treatment Decision in Belgium

Start: Jun 2019Est. completion: Oct 2019215 patients
N/ACompleted

Related Jobs in Oncology

Phase Legend

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

Key Insights

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.