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Hepatocellular Carcinoma Non-resectable

Oncology
2
Pipeline Programs
8
Companies
10
Clinical Trials
2 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
1
0
1
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
2100%
+ 8 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

Abbott
AbbottABBOTT PARK, IL
1 program
1
ABT-869Phase 31 trial
Active Trials
NCT01009593Terminated1,035Est. Jul 2012
Boston Scientific
Boston ScientificCA - Valencia
1 program
1
Selective Internal RadiotherapyPhase 21 trial
Active Trials
NCT07122089Not Yet Recruiting80Est. Jan 2030
HaploX Biotechnology
HaploX BiotechnologyChina - Shenzhen
2 programs
HAICN/A1 trial
TACEN/A1 trial
Active Trials
NCT05713994Recruiting300Est. Dec 2025
NCT05717738Recruiting300Est. Dec 2024
Jeil Pharmaceutical
Jeil PharmaceuticalKorea - Seoul
2 programs
UNI-DEBN/A1 trial
UNI-DEBN/A1 trial
Active Trials
NCT03533920Completed62Est. Sep 2018
NCT03564405Completed10Est. May 2017
Terumo Medical
Terumo MedicalGermany - Leverkusen
1 program
Holmium-166 radioembolizationN/A1 trial
Active Trials
NCT05114148Unknown30Est. Nov 2025
ImmunityBio
ImmunityBioSAN DIEGO, CA
1 program
ETBX-011PHASE_1_21 trial
Active Trials
NCT03563170Withdrawn0Est. Aug 2019
Eisai
EisaiChina - Liaoning
1 program
LenvatinibPHASE_1_2Small Molecule1 trial
Active Trials
NCT05901194Active Not Recruiting25Est. Apr 2027
Ipsen
IpsenChina - Tianjin
1 program
CabozantinibPHASE_2Small Molecule1 trial
Active Trials
NCT04511455Completed22Est. Dec 2024

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
AbbottABT-869
Boston ScientificSelective Internal Radiotherapy
IpsenCabozantinib
EisaiLenvatinib
ImmunityBioETBX-011
Terumo MedicalHolmium-166 radioembolization
HaploX BiotechnologyTACE
HaploX BiotechnologyHAIC
Jeil PharmaceuticalUNI-DEB
Jeil PharmaceuticalUNI-DEB

Clinical Trials (10)

Total enrollment: 1,864 patients across 10 trials

Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellular Carcinoma (HCC)

Start: Jan 2010Est. completion: Jul 20121,035 patients
Phase 3Terminated
NCT07122089Boston ScientificSelective Internal Radiotherapy

Evaluation of SIRT Followed by Immunotherapy for Treatment of Hepatocellular Carcinoma With Portal Vein Thrombosis

Start: Jan 2026Est. completion: Jan 203080 patients
Phase 2Not Yet Recruiting
NCT04511455IpsenCabozantinib

Cabozantinib for Patients with Hepatocellular Carcinoma (HCC) Refractory to First Line Treatment

Start: Dec 2020Est. completion: Dec 202422 patients
Phase 2Completed

Lenvatinib Treatment in Waiting List of Liver Transplantation After TACE Failure in Patients With Hepatocellular Carcinoma

Start: Jul 2024Est. completion: Apr 202725 patients
Phase 1/2Active Not Recruiting

QUILT-3.072: NANT Hepatocellular Carcinoma (HCC) Vaccine

Start: May 2018Est. completion: Aug 20190
Phase 1/2Withdrawn
NCT05114148Terumo MedicalHolmium-166 radioembolization

Individualized Dosimetry for Holmium-166-radioembolization in Patients With Unresectable Hepatocellular Carcinoma

Start: Mar 2022Est. completion: Nov 202530 patients
N/AUnknown

Combined TACE, TKI/Anti-VEGF and ICIs as Conversion Therapy for Advanced Hepatocellular Carcinoma

Start: Jan 2022Est. completion: Dec 2024300 patients
N/ARecruiting

Combined HAIC, TKI/Anti-VEGF and ICIs as Conversion Therapy for Unresectable Hepatocellular Carcinoma

Start: May 2020Est. completion: Dec 2025300 patients
N/ARecruiting

Clinical Trial to Evaluate the Efficacy and Safety of UNI-DEB for Unresectable Hepatocellular Carcinoma

Start: Oct 2017Est. completion: Sep 201862 patients
N/ACompleted

Pilot Clinical Trial to Evaluate the UNI-DEB for Unresectable Hepatocellular Carcinoma

Start: Dec 2016Est. completion: May 201710 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

1 late-stage (Phase 3) programs, potential near-term approvals
2 actively recruiting trials targeting 1,864 patients
8 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.