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Penile Cancer

Oncology
2
Pipeline Programs
4
Companies
15
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
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
2100%
+ 1 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

3 companies ranked by most advanced pipeline stage

Pfizer
PfizerNEW YORK, NY
1 program
1
AvelumabPhase 2Monoclonal Antibody5 trials
Active Trials
NCT04841148Recruiting96Est. May 2028
NCT03964532Active Not Recruiting24Est. Apr 2027
NCT03774901Unknown32Est. Sep 2024
+2 more trials
Incyte
IncyteDE - Wilmington
1 program
1
RetifanlimabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT04231981Completed18Est. Aug 2022
Lepu Biopharma
Lepu BiopharmaChina - Shanghai
1 program
MRG003PHASE_11 trial
Active Trials
NCT07054307Not Yet RecruitingEst. Jul 2030

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
PfizerAvelumab
PfizerAvelumab
IncyteRetifanlimab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab
Lepu BiopharmaMRG003
PfizerAvelumab
PfizerAvelumab
PfizerAvelumab

Clinical Trials (15)

Total enrollment: 1,218 patients across 15 trials

Avelumab and Talazoparib in Untreated Advanced Ovarian Cancer (JAVELIN OVARIAN PARP 100)

Start: Jul 2018Est. completion: Dec 202179 patients
Phase 3Terminated

Avelumab or Hydroxychloroquine With or Without Palbociclib to Eliminate Dormant Breast Cancer

Start: Jun 2021Est. completion: May 202896 patients
Phase 2Recruiting
NCT04231981IncyteRetifanlimab

Efficacy of INCMGA00012 in Penile Squamous Cell Carcinoma (ORPHEUS)

Start: Apr 2020Est. completion: Aug 202218 patients
Phase 2Completed

Maintenance Avelumab Immunotherapy in Patients With Locally Advanced or Metastatic Squamous Cell Penile Carcinoma

Start: Mar 2019Est. completion: Sep 202432 patients
Phase 2Unknown

Neoadjuvant Endocrine Therapy, Palbociclib, Avelumab in Estrogen Receptor Positive Breast Cancer

Start: Nov 2018Est. completion: Dec 202633 patients
Phase 2Active Not Recruiting

Javelin BRCA/ATM: Avelumab Plus Talazoparib in Patients With BRCA or ATM Mutant Solid Tumors

Start: Jun 2018Est. completion: Feb 2023202 patients
Phase 2Terminated

Palbociclib After CDK and Endocrine Therapy (PACE)

Start: Sep 2017Est. completion: Jun 2026220 patients
Phase 2Active Not Recruiting

TALAVE: Induction Talazoparib Followed by Combination of Talazoparib and Avelumab in Advanced Breast Cancer

Start: Apr 2019Est. completion: Apr 202724 patients
Phase 1/2Active Not Recruiting

Javelin Parp Medley: Avelumab Plus Talazoparib In Locally Advanced Or Metastatic Solid Tumors

Start: Oct 2017Est. completion: Jan 2023223 patients
Phase 1/2Terminated

Study to Evaluate Safety, Efficacy, Pharmacokinetics And Pharmacodynamics Of Avelumab In Combination With Either Crizotinib Or PF-06463922 In Patients With NSCLC. (Javelin Lung 101)

Start: Dec 2015Est. completion: Jul 202243 patients
Phase 1/2Terminated

Study For Patients With NSCLC EGFR Mutations (Del 19 or L858R +/- T790M)

Start: May 2015Est. completion: May 202065 patients
Phase 1/2Terminated

MRG003 Plus HX008 as First-Line Treatment for EGFR-Positive Locally Advanced or Metastatic Penile Squamous Cell Carcinoma

Start: Jul 2025Est. completion: Jul 2030
Phase 1Not Yet Recruiting

A Combination of Avelumab and Taxane (AVETAX) for Urothelial Cancer

Start: Oct 2018Est. completion: Feb 202421 patients
Phase 1Completed

Avelumab, Cetuximab, and Palbociclib in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Start: Jun 2018Est. completion: Dec 202524 patients
Phase 1Active Not Recruiting

A Study Of PF-06647020 For Adult Patients With Advanced Solid Tumors

Start: Oct 2014Est. completion: Nov 2019138 patients
Phase 1Completed

Related Jobs in Oncology

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 1,218 patients
Monoclonal Antibody is the dominant modality (100% of programs)
4 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.