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Stomach Neoplasms

Oncology
17
Pipeline Programs
18
Companies
20
Clinical Trials
1
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
6
1
4
0
5
1
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
770%
Small Molecule
330%
+ 17 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.

On Market (1)

Approved therapies currently available

Merck & Co.
KEYTRUDAApproved
pembrolizumab
Merck & Co.
Programmed Death Receptor-1 Blocking Antibody [EPC]intravenous2014
117M Part D

Competitive Landscape

17 companies ranked by most advanced pipeline stage

Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
1
PembrolizumabPHASE_3Monoclonal Antibody
MSD
MSDIreland - Ballydine
2 programs
2
PembrolizumabPhase 3Monoclonal Antibody
PembrolizumabPhase 3Monoclonal Antibody
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
2 programs
2
PembrolizumabPhase 3Monoclonal Antibody1 trial
PembrolizumabPhase 3Monoclonal Antibody1 trial
Active Trials
NCT04859582Withdrawn0Est. Nov 2024
NCT03675737Completed1,579Est. Mar 2025
LintonPharm
LintonPharmChina - Guangzhou
1 program
1
CatumaxomabPhase 3Monoclonal Antibody1 trial
Active Trials
NCT04222114Unknown282Est. Aug 2023
Pfizer
PfizerNEW YORK, NY
4 programs
3
1
SunitinibPhase 2Small Molecule1 trial
5-fluorouracilPhase 11 trial
axitinibPhase 1Small Molecule1 trial
capecitabinePhase 11 trial
Active Trials
NCT00555672Completed34Est. Aug 2010
NCT00842244Completed22Est. Oct 2012
NCT00555620Completed76Est. Dec 2011
+1 more trials
UNION therapeutics
UNION therapeuticsDenmark - Hellerup
3 programs
1
FruquintinibPhase 2Small Molecule1 trial
Enhanced Magnifying Endoscopy for Diagnosis of Early Gastric CancerN/A1 trial
The intervention groupN/A1 trial
Active Trials
NCT01617876Completed282Est. Mar 2012
NCT04985084Completed35Est. Aug 2022
NCT05625737Unknown29Est. Sep 2025
Amgen
AmgenTHOUSAND OAKS, CA
2 programs
1
1
AMG 337Phase 21 trial
AMG 337Phase 1/21 trial
Active Trials
NCT02096666Completed11Est. Dec 2018
NCT02016534Terminated60Est. Oct 2016
Martin Pharmaceuticals
1 program
1
docetaxel, oxaliplatin, capecitabinePhase 21 trial
Active Trials
NCT00511446Completed56Est. Jan 2013
Exelixis
ExelixisCA - Alameda
1 program
1
BMS-833923Phase 1
CELLID
CELLIDKorea - Seoul
1 program
1
BVAC-BPhase 11 trial
Active Trials
NCT03425773Completed8Est. May 2019
Prevail Therapeutics
1 program
1
RamucirumabPhase 1Monoclonal Antibody1 trial
Active Trials
NCT02359058Completed18Est. Nov 2016
Sanofi
SanofiPARIS, France
3 programs
DocetaxelPHASE_21 trial
Docetaxel, Cisplatin, Fluorouracil, Bevacizumab, LeucovorinPHASE_2
CapecitabinePHASE_31 trial
Active Trials
NCT00343239Completed59Est. Mar 2012
NCT00087958Completed168Est. Apr 2009
Coordination Pharmaceuticals
1 program
OLGA and OLGIM Stage System for Gastric CancerN/A1 trial
Active Trials
NCT03380052Completed2,900Est. Jan 2022
GSK
GSKLONDON, United Kingdom
1 program
Tumor Markers Study in Gastric Cancer for Cancer Immunotherapy (ONCO-RD 010 CRT)N/A1 trial
Active Trials
NCT02686424Suspended250
ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
Tumor Markers Study in Gastric Cancer for Cancer Immunotherapy (ONCO-RD 010 CRT)N/A
Roche
RocheSTAVANGER NORWAY, Norway
1 program
CapecitabinePHASE_3
Ortho Development
1 program
epoetin alfaPHASE_31 trial
Active Trials
NCT00036400Completed60Est. Dec 2003

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
LintonPharmCatumaxomab
Sharp TherapeuticsPembrolizumab
Sharp TherapeuticsPembrolizumab
Ortho Developmentepoetin alfa
UNION therapeuticsFruquintinib
AmgenAMG 337
Martin Pharmaceuticalsdocetaxel, oxaliplatin, capecitabine
SanofiDocetaxel
PfizerSunitinib
SanofiCapecitabine
AmgenAMG 337
CELLIDBVAC-B
Prevail TherapeuticsRamucirumab
Pfizeraxitinib
Pfizer5-fluorouracil

Showing 15 of 20 trials with date data

Clinical Trials (20)

Total enrollment: 6,007 patients across 20 trials

Comparing the Efficacy and Safety of Intra-peritoneal Infusion of Catumaxomab and Treatment of Investigator Choice in Patients With Advanced Gastric Carcinoma With Peritoneal Metastasis

Start: Oct 2020Est. completion: Aug 2023282 patients
Phase 3Unknown

Pembrolizumab (MK-3475) Plus Chemotherapy Versus Placebo Plus Chemotherapy in Participants Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma (MK-3475-859/KEYNOTE-859)

Start: Nov 2018Est. completion: Mar 20251,579 patients
Phase 3Completed

Pembrolizumab (MK-3475) Plus Chemotherapy Versus Placebo Plus Chemotherapy in Participants Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma (MK-3475-859/KEYNOTE-859)-China Extension

Start: Nov 2018Est. completion: Nov 20240
Phase 3Withdrawn

Study of the Efficacy and Safety of Epoetin Alfa Administered Weekly in Patients With Gastric or Rectal Cancers Undergoing a Treatment Plan of Preoperative Chemotherapy and Radiation Therapy, Followed by Surgery

Start: Dec 2001Est. completion: Dec 200360 patients
Phase 3Completed

Fruquintinib Combined with Sintilimab As Second-line Therapy for Gastric or Gastro-esophageal Junction Adenocarcinoma

Start: Sep 2022Est. completion: Sep 202529 patients
Phase 2Unknown

Phase 2 Study of AMG 337 in MET Amplified Gastric/Esophageal Adenocarcinoma or Other Solid Tumors

Start: Feb 2014Est. completion: Oct 201660 patients
Phase 2Terminated
NCT00511446Martin Pharmaceuticalsdocetaxel, oxaliplatin, capecitabine

Trial of Docetaxel, Oxaliplatin and Capecitabine (TEX) in Advanced or Metastatic Gastric Cancer

Start: Aug 2007Est. completion: Jan 201356 patients
Phase 2Completed

Docetaxel in Locally Advanced Gastric Adenocarcinoma

Start: Jun 2006Est. completion: Mar 201259 patients
Phase 2Completed

An International Phase 2 Study Of SU011248 In Patients With Advanced / Metastatic Gastric Cancer Failing Chemotherapy

Start: Jan 2006Est. completion: May 200878 patients
Phase 2Completed
NCT00087958SanofiCapecitabine

Intravenous RPR109881 in Male or Female Patients With Advanced Breast Cancer Who no Longer Respond to Anthracycline, Taxane and Capecitabine Treatment

Start: Aug 2004Est. completion: Apr 2009168 patients
Phase 2Completed

A Phase 1/2 Study Evaluating AMG 337 in Asian Subjects

Start: Apr 2014Est. completion: Dec 201811 patients
Phase 1/2Completed

Safety and Tolerability Evaluation Study of BVAC-B in Patients With HER2/Neu(Human Epithelial Growth Factor Receptor 2) Positive Gastric Cancer After Failure to Standard Care

Start: Feb 2018Est. completion: May 20198 patients
Phase 1Completed

A Study of Ramucirumab Combination Therapy in Japanese Participants Who Have Advanced Stomach Cancer

Start: Feb 2015Est. completion: Nov 201618 patients
Phase 1Completed

Study Of Axitinib In Combination With Cisplatin And Capecitabine In Patients With Advanced Gastric Cancer

Start: Apr 2009Est. completion: Oct 201222 patients
Phase 1Completed
NCT00555672Pfizer5-fluorouracil

Study Of Sunitinib In Combination With Cisplatin And 5-Fluorouracil In Patients With Advanced Gastric Cancer

Start: Aug 2008Est. completion: Aug 201034 patients
Phase 1Completed
NCT00555620Pfizercapecitabine

Study Of Sunitinib In Combination With Cisplatin/Capecitabine Or Oxaliplatin/Capecitabine In Patients With Advanced Gastric Cancer

Start: May 2008Est. completion: Dec 201176 patients
Phase 1Completed
NCT04985084UNION therapeuticsThe intervention group

Development and Testing of a Social Cognitive Theory-based Dietary Behavioral Intervention in Gastric Cancer Survivors

Start: Jan 2022Est. completion: Aug 202235 patients
N/ACompleted
NCT02686424GSKTumor Markers Study in Gastric Cancer for Cancer Immunotherapy (ONCO-RD 010 CRT)

Tumor Markers Study in Gastric Cancer for Cancer Immunotherapy (ONCO-RD 010 CRT)

Start: Mar 2010250 patients
N/ASuspended
NCT01617876UNION therapeuticsEnhanced Magnifying Endoscopy for Diagnosis of Early Gastric Cancer

Enhanced Magnifying Endoscopy for Diagnosis of Early Gastric Cancer

Start: Mar 2010Est. completion: Mar 2012282 patients
N/ACompleted
NCT03380052Coordination PharmaceuticalsOLGA and OLGIM Stage System for Gastric Cancer

OLGA and OLGIM Stage System for Gastric Cancer

Start: Feb 2006Est. completion: Jan 20222,900 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

5 late-stage (Phase 3) programs, potential near-term approvals
18 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.