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Neuroendocrine Carcinoma

Oncology
8
Pipeline Programs
8
Companies
9
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
1
1
6
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
583%
Peptide
117%
+ 5 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

Sandoz
SandozAustria - Kundl
4 programs
4
AvastinPhase 21 trial
EverolimusPhase 21 trial
Octreotide LARPhase 2Peptide1 trial
RAD001Phase 21 trial
Active Trials
NCT00607113Completed41Est. Oct 2011
NCT02687958Unknown30Est. Dec 2023
NCT01886287Terminated2Est. Oct 2014
+1 more trials
MSD
MSDIreland - Ballydine
1 program
1
PembrolizumabPhase 2Monoclonal Antibody
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
PembrolizumabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT03901378Withdrawn0Est. Jan 2021
UNION therapeutics
UNION therapeuticsDenmark - Hellerup
1 program
1
Surufatinib and SerplulimabPhase 1/2Monoclonal Antibody1 trial
Active Trials
NCT05747729Unknown60Est. Feb 2026
Seneca Therapeutics
Seneca TherapeuticsPA - Blue Bell
1 program
1
Seneca Valley Virus-001Phase 11 trial
Active Trials
NCT06889493Recruiting36Est. Jun 2030
RadioMedix
RadioMedixTX - Houston
1 program
68Ga-DOTATATEN/A1 trial
Active Trials
NCT01879657Completed169Est. Dec 2017
Qilu Pharmaceutical
Qilu PharmaceuticalChina - Jinan
1 program
Nab-paclitaxel Combined With BevacizumabPHASE_2Monoclonal Antibody1 trial
Active Trials
NCT04705519Completed79Est. Sep 2024
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
PembrolizumabPHASE_2Monoclonal Antibody

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
Qilu PharmaceuticalNab-paclitaxel Combined With Bevacizumab
Sharp TherapeuticsPembrolizumab
SandozEverolimus
SandozOctreotide LAR
SandozAvastin
SandozRAD001
UNION therapeuticsSurufatinib and Serplulimab
Seneca TherapeuticsSeneca Valley Virus-001
RadioMedix68Ga-DOTATATE

Clinical Trials (9)

Total enrollment: 484 patients across 9 trials

NCT04705519Qilu PharmaceuticalNab-paclitaxel Combined With Bevacizumab

Nab-paclitaxel Combined with Bevacizumab in the Treatment of Metastatic Extrapulmonary Neuroendocrine Carcinoma

Start: Jan 2021Est. completion: Sep 202479 patients
Phase 2Completed

Pembrolizumab With Chemotherapy in Metastatic or Unresectable High Grade Gastroenteropancreatic or Lung Neuroendocrine Carcinoma

Start: Oct 2019Est. completion: Jan 20210
Phase 2Withdrawn

Study of Everolimus as Maintenance Therapy for Metastatic NEC With Pulmonary or Gastroenteropancreatic Origin

Start: May 2015Est. completion: Dec 202330 patients
Phase 2Unknown
NCT01886287SandozOctreotide LAR

P:II Above-Label Octreotide-LAR With Insufficiently Controlled Carcinoid Syndrome

Start: Dec 2013Est. completion: Oct 20142 patients
Phase 2Terminated

Avastin (Bevacizumab) and RAD001 (Everolimus) in Advanced Low or Intermediate Grade Neuroendocrine Carcinoma

Start: Jan 2008Est. completion: Oct 201141 patients
Phase 2Completed

RAD001 Plus Octreotide Depot in Metastatic or Unresectable Low Grade Neuroendocrine Carcinoma

Start: Jan 2005Est. completion: Jul 200967 patients
Phase 2Completed
NCT05747729UNION therapeuticsSurufatinib and Serplulimab

A Single-arm, Open-label, Clinical Trial of Surufatinib/Serplulimab/Platinum/Etoposide in Neuroendocrine Carcinoma.

Start: Feb 2023Est. completion: Feb 202660 patients
Phase 1/2Unknown
NCT06889493Seneca TherapeuticsSeneca Valley Virus-001

SVV-001 With Nivolumab and Ipilimumab in Patients With Poorly Differentiated Neuroendocrine Carcinomas (NEC) or Well-Differentiated High-Grade Neuroendocrine Tumors (NET)

Start: May 2025Est. completion: Jun 203036 patients
Phase 1Recruiting

68Ga-DOTATATE PET-CT for Diagnosis of Neuroendocrine Tumors (NETs)

Start: Mar 2013Est. completion: Dec 2017169 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 actively recruiting trials targeting 484 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.