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Gastrointestinal Stromal Tumor

Oncology
6
Pipeline Programs
8
Companies
23
Clinical Trials
0
Approved Products

Pipeline by Development Stage

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

Drug Modality Breakdown

Small Molecule
375%
Monoclonal Antibody
125%
+ 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·Launch14.6yr
#2FARXIGAStable
$4.3B
AstraZeneca·Peak15.0yr
#3REVLIMIDDeclining
$3.9B
Bristol Myers Squibb·LOE Approaching1.4yr
#4XTANDIStable
$2.6B
Astellas·Peak10.4yr
#5IMBRUVICAStable
$2.4B
AbbVie·Peak8.5yr

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

Pfizer
PfizerNEW YORK, NY
2 programs
1
1
sunitinib malatePhase 31 trial
SunitinibPhase 1Small Molecule
Active Trials
NCT00372567Terminated69Est. Nov 2009
Sandoz
SandozAustria - Kundl
3 programs
2
AUY922Phase 2
NilotinibPhase 2Small Molecule
GlivecN/A
Innovation Pharmaceuticals
1 program
1
imatinib mesylatePhase 21 trial
Active Trials
NCT00764595Completed5Est. Mar 2016
Oregon Therapeutics
Oregon TherapeuticsFrance - Paris
1 program
1
regorafenibPhase 2Small Molecule
Novartis
NovartisBASEL, Switzerland
2 programs
GlivecN/A1 trial
AUY922PHASE_25 trials
Active Trials
NCT01613053No Longer Available
NCT01784640Completed13Est. Oct 2018
NCT01772797Completed22Est. Jan 2016
+3 more trials
Alliance Pharmaceuticals
1 program
mutation analysisN/A1 trial
Active Trials
NCT00954655Completed1Est. Apr 2013
Mendus
MendusSweden - Stockholm
1 program
IntuvaxPHASE_11 trial
Active Trials
NCT02686944Completed6Est. May 2019
Bristol Myers Squibb
1 program
IpilimumabPHASE_2Monoclonal Antibody1 trial
Active Trials
NCT02880020Completed36Est. Aug 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Pfizersunitinib malate
Bristol Myers SquibbIpilimumab
NovartisAUY922
NovartisAUY922
NovartisAUY922
NovartisAUY922
NovartisAUY922
NovartisAUY922
NovartisAUY922
NovartisAUY922
Innovation Pharmaceuticalsimatinib mesylate
NovartisAUY922
NovartisAUY922
NovartisAUY922
MendusIntuvax

Showing 15 of 22 trials with date data

Clinical Trials (23)

Total enrollment: 810 patients across 23 trials

NCT00372567Pfizersunitinib malate

Safety And Effectiveness Of Daily Dosing With Sunitinib Or Imatinib In Patients With Gastrointestinal Stromal Tumors

Start: Jun 2007Est. completion: Nov 200969 patients
Phase 3Terminated

Nivolumab With or Without Ipilimumab in Treating Patients With Gastrointestinal Stromal Tumor That Is Metastatic or Cannot Be Removed by Surgery

Start: Dec 2016Est. completion: Aug 202236 patients
Phase 2Completed

An Open-label, Randomized Phase II Study to Evaluate the Efficacy of AUY922 vs Pemetrexed or Docetaxel in NSCLC Patients With EGFR Mutations

Start: Nov 2012Est. completion: Nov 201559 patients
Phase 2Terminated

HSP90 Inhibitor, AUY922, in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera Myelofibrosis (Post-PV MF), Post-Essential Thrombocythemia Myelofibrosis (Post-ET MF), and Refractory PV/ET

Start: Aug 2012Est. completion: May 20157 patients
Phase 2Terminated

A Study of the HSP90 Inhibitor AUY922

Start: Aug 2012Est. completion: Nov 201521 patients
Phase 2Terminated

Study of AUY922 in Metastatic Pancreatic Cancer Who Are Resistant to First Line Chemotherapy

Start: Jan 2012Est. completion: Aug 201315 patients
Phase 2Terminated

Study of Hsp90 Inhibitor AUY922 for the Treatment of Patients With Refractory Gastrointestinal Stromal Tumor

Start: Dec 2011Est. completion: Feb 201525 patients
Phase 2Completed

Phase II of AUY922 in Second-line Gastric Cancer in Combination With Trastuzumab in HER2 Positive Patients

Start: Nov 2011Est. completion: Jun 201321 patients
Phase 2Terminated

A Study of AUY922 in Non-small-cell Lung Cancer Patients Who Have Received Previous Two Lines of Chemotherapy.

Start: Oct 2010Est. completion: Aug 2014153 patients
Phase 2Completed

Phase II Trial of AUY922 vs. Comparators in Advanced Gastric Cancer

Start: Apr 2010Est. completion: May 201268 patients
Phase 2Completed

Imatinib Mesylate in Treating Patients With Liver Metastasis From a Gastrointestinal Stromal Tumor

Start: Oct 2008Est. completion: Mar 20165 patients
Phase 2Completed

Combination of AUY922 With Trastuzumab in HER2+ Advanced Breast Cancer Patients Previously Treated With Trastuzumab

Start: Sep 2010Est. completion: Oct 201345 patients
Phase 1/2Completed

A Phase I-Ib/II Study to Determine the Maximum Tolerated Dose (MTD) of AUY922 Alone and in Combination With Bortezomib, With or Without Dexamethasone, in Patients With Relapsed or Refractory Multiple Myeloma.

Start: Jul 2008Est. completion: Jan 201129 patients
Phase 1/2Completed

Phase I-II Study to Determine the Maximum Tolerated Dose (MTD) of AUY922 in Advanced Solid Malignancies, and Efficacy in HER2+ or ER+ Locally Advanced or Metastatic Breast Cancer Patients

Start: Jul 2007Est. completion: Apr 2012117 patients
Phase 1/2Completed

A Study to Evaluate the Safety of Intuvax Administered Intra-tumorally in Patients With Gastrointestinal Stromal Tumors

Start: Jun 2016Est. completion: May 20196 patients
Phase 1Completed

Pemetrexed Disodium and Hsp90 Inhibitor AUY922 in Treating Patients With Previously Treated Stage IV Non-Small Cell Lung Cancer

Start: Jan 2014Est. completion: Oct 201813 patients
Phase 1Completed

Phase Ib Study of LDK378 and AUY922 in ALK-rearranged Non-small Cell Lung Cancer

Start: Jun 2013Est. completion: Jan 201622 patients
Phase 1Completed

PI3K Inhibitor BYL719 in Combination With the HSP90 Inhibitor AUY922 in Patients With Advanced or Metastatic Gastric Cancer

Start: Dec 2012Est. completion: Mar 201418 patients
Phase 1Completed

Study of AUY922 and Cetuximab in Patients With KRAS Wild-Type Metastatic Colorectal Cancer

Start: Feb 2011Est. completion: May 201520 patients
Phase 1Completed

A Study of the Hsp90 Inhibitor AUY922 Plus Capecitabine for the Treatment of Patients With Advanced Solid Tumors

Start: Nov 2010Est. completion: Jun 201423 patients
Phase 1Completed

Dose Escalation Study of AUY922 in Advanced Solid Malignancies in Japan

Start: Nov 2008Est. completion: May 201237 patients
Phase 1Completed

Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination

N/ANo Longer Available

Study of Tumor Samples in Patients Undergoing Treatment for Gastrointestinal Stromal Tumors on Clinical Trial ACOSOG-Z9001

Start: Dec 2008Est. completion: Apr 20131 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
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.