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Classical Hodgkin Lymphoma

Oncology
9
Pipeline Programs
11
Companies
9
Clinical Trials
3 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
1
7
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
788%
Small Molecule
113%
+ 6 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

9 companies ranked by most advanced pipeline stage

Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
3 programs
3
Computed TomographyPhase 21 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT03226249Unknown30Est. Oct 2024
NCT05008224Completed146Est. May 2024
NCT05404945Recruiting44Est. Oct 2027
MSD
MSDIreland - Ballydine
3 programs
3
Computed TomographyPhase 2
PembrolizumabPhase 2Monoclonal Antibody
PembrolizumabPhase 2Monoclonal Antibody
Gloria Biosciences
Gloria BiosciencesChina - Guangzhou
1 program
1
Zimberelimab 240mgPhase 21 trial
Active Trials
NCT05900765Recruiting54Est. Jun 2026
Genmab
GenmabNetherlands - Utrecht
1 program
1
GEN3017Phase 1/21 trial
Active Trials
NCT06018129Terminated9Est. Feb 2025
Rhizen Pharmaceuticals
Rhizen PharmaceuticalsSwitzerland - Basel
1 program
1
TenalisibPhase 1Small Molecule1 trial
Active Trials
NCT03471351Terminated2Est. Feb 2019
ETS
ETSMO - Rolla
2 programs
Lifestyles Implemented-Survivorship Care PlanN/A1 trial
Treatment for clinical practiseN/A1 trial
Active Trials
NCT05934084Recruiting552Est. Feb 2026
NCT03552003Unknown400Est. Jan 2026
Bristol Myers Squibb
1 program
NivolumabPHASE_1Monoclonal Antibody1 trial
Active Trials
NCT05352828Active Not Recruiting15Est. Dec 2037
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
PembrolizumabPHASE_2Monoclonal Antibody
BeOne Medicines
BeOne MedicinesCA - San Carlos
1 program
TislelizumabPHASE_3Monoclonal Antibody

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
Gloria BiosciencesZimberelimab 240mg
Sharp TherapeuticsPembrolizumab
Sharp TherapeuticsPembrolizumab
Sharp TherapeuticsComputed Tomography
GenmabGEN3017
Bristol Myers SquibbNivolumab
Rhizen PharmaceuticalsTenalisib
ETSLifestyles Implemented-Survivorship Care Plan
ETSTreatment for clinical practise

Clinical Trials (9)

Total enrollment: 1,252 patients across 9 trials

A Study of Zimberelimab(GLS-010) Combined With AVD for Newly Diagnosed Early-stage Hodgkin's Lymphoma

Start: Jun 2023Est. completion: Jun 202654 patients
Phase 2Recruiting

Fitness-adapted, Pembrolizumab-based Therapy for Untreated Classical Hodgkin Lymphoma Patients 60 Years of Age and Above

Start: Jul 2022Est. completion: Oct 202744 patients
Phase 2Recruiting

Study of Safety and Efficacy of Pembrolizumab and Chemotherapy in Participants With Newly Diagnosed Classical Hodgkin Lymphoma (cHL) (MK-3475-C11/KEYNOTE-C11)

Start: Oct 2021Est. completion: May 2024146 patients
Phase 2Completed

PET-Directed Therapy With Pembrolizumab and Combination Chemotherapy in Treating Patients With Previously Untreated Classical Hodgkin Lymphoma

Start: Nov 2017Est. completion: Oct 202430 patients
Phase 2Unknown

A First-in-human Trial of GEN3017 in Hodgkin Lymphoma and Non-Hodgkin Lymphoma

Start: Sep 2023Est. completion: Feb 20259 patients
Phase 1/2Terminated

Autologous CD30.CAR-T in Combination With Nivolumab in cHL Patients After Failure of Frontline Therapy

Start: Jul 2022Est. completion: Dec 203715 patients
Phase 1Active Not Recruiting

Safety and Efficacy Study of Tenalisib (RP6530) in Combination With Pembrolizumab in Relapsed or Refractory cHL

Start: Jul 2018Est. completion: Feb 20192 patients
Phase 1Terminated
NCT05934084ETSLifestyles Implemented-Survivorship Care Plan

Lifestyles Implemented-Survivorship Care Plan In Lymphoma Survivors

Start: Feb 2024Est. completion: Feb 2026552 patients
N/ARecruiting
NCT03552003ETSTreatment for clinical practise

Study for Elderly (≥ 65 Years) Patients With Classical Hodgkin Lymphoma Undergoing CGA at Diagnosis

Start: Aug 2018Est. completion: Jan 2026400 patients
N/AUnknown

Related Jobs in Oncology

Phase Legend

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

Key Insights

3 actively recruiting trials targeting 1,252 patients
Monoclonal Antibody is the dominant modality (88% of programs)
11 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.