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Metastatic Pancreatic Ductal Adenocarcinoma

Oncology
13
Pipeline Programs
17
Companies
20
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
3
1
7
0
2
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
467%
Monoclonal Antibody
233%
+ 14 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

16 companies ranked by most advanced pipeline stage

Sandoz
SandozAustria - Kundl
3 programs
1
1
1
NIS793Phase 31 trial
NIS793Phase 21 trial
Canakinumab injection; spartalizumab, nab-paclitaxel, gemcitabinePhase 11 trial
Active Trials
NCT04581343Completed10Est. Feb 2023
NCT04390763Terminated164Est. May 2024
NCT04935359Completed511Est. Aug 2024
Taiho Pharma
Taiho PharmaJapan - Tokyo
1 program
1
QuemliclustatPhase 3Small Molecule
MSD
MSDIreland - Ballydine
2 programs
2
BXCL701Phase 21 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT05558982Active Not Recruiting22Est. Nov 2027
NCT04666740Active Not Recruiting63Est. Jan 2027
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
2 programs
2
BXCL701Phase 2
PembrolizumabPhase 2Monoclonal Antibody
BioXcel Therapeutics
BioXcel TherapeuticsCT - New Haven
1 program
1
BXCL701Phase 2
Pfizer
PfizerNEW YORK, NY
1 program
1
PF-04136309Phase 21 trial
Active Trials
NCT02732938Terminated22Est. Oct 2017
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
MEDI4736 in combination with nab-paclitaxel and gemcitabinePhase 1/21 trial
Active Trials
NCT02583477Completed23Est. Jul 2018
Cantargia
CantargiaSweden - Lund
1 program
1
CAN04Phase 11 trial
Active Trials
NCT04990037Completed25Est. Jun 2023
Aclaris Therapeutics
Aclaris TherapeuticsMO - St. Louis
1 program
1
zunsemetinibPhase 1Small Molecule1 trial
Active Trials
NCT06648434Recruiting51Est. May 2030
Lonza
LonzaBasel, Switzerland
1 program
Autologous Mesothelin-specific TCR-T CellsPHASE_11 trial
Active Trials
NCT04809766Terminated9Est. Jan 2025
Alligator Bioscience
1 program
CD40 agonist mitazalimab in combination with chemotherapyPHASE_1_21 trial
Active Trials
NCT04888312Active Not Recruiting94Est. Jun 2026
Bristol Myers Squibb
1 program
OFFPHASE_25 trials
Active Trials
NCT05953402Not Yet Recruiting1,182Est. Jun 2033
NCT06710470Active Not Recruiting833Est. Feb 2029
NCT05170126Recruiting1,182Est. Jun 2032
+2 more trials
Chipscreen Biosciences
Chipscreen BiosciencesChina - Shenzhen
1 program
ChiauranibPHASE_3Small Molecule1 trial
Active Trials
NCT07445295Not Yet Recruiting558Est. Nov 2028
GSK
GSKLONDON, United Kingdom
1 program
MomelotinibPHASE_3Small Molecule1 trial
Active Trials
NCT02101021Terminated25Est. Apr 2017
Corcept Therapeutics
Corcept TherapeuticsCA - Redwood City
1 program
Relacorilant, 100 mg and 25 mgPHASE_31 trial
Active Trials
NCT04329949Terminated43Est. Mar 2022
Chia Tai TianQing Pharmaceutical Group
1 program
TQB2868 InjectionPHASE_31 trial
Active Trials
NCT07165951Recruiting566Est. Dec 2028

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
Bristol Myers SquibbOFF
Chipscreen BiosciencesChiauranib
Chia Tai TianQing Pharmaceutical GroupTQB2868 Injection
SandozNIS793
Corcept TherapeuticsRelacorilant, 100 mg and 25 mg
GSKMomelotinib
MSDBXCL701
MSDPembrolizumab
SandozNIS793
Bristol Myers SquibbOFF
PfizerPF-04136309
Alligator BioscienceCD40 agonist mitazalimab in combination with chemotherapy
AstraZenecaMEDI4736 in combination with nab-paclitaxel and gemcitabine
Aclaris Therapeuticszunsemetinib
LonzaAutologous Mesothelin-specific TCR-T Cells

Showing 15 of 20 trials with date data

Clinical Trials (20)

Total enrollment: 5,450 patients across 20 trials

Precision Medicine Offers Belatacept Monotherapy

Start: Feb 2019Est. completion: Dec 20220
Phase 4Withdrawn

Chiauranib Plus PD-1 Inhibitor, Albumin-paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

Start: Mar 2026Est. completion: Nov 2028558 patients
Phase 3Not Yet Recruiting

Clinical Trial Comparing TQB2868 Injection Combined With Anlotinib Hydrochloride Capsules With Placebo Combined With Chemotherapy as First-line Treatment for Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC)

Start: Dec 2025Est. completion: Dec 2028566 patients
Phase 3Recruiting

Study of Efficacy and Safety of NIS793 in Combination With Standard of Care (SOC) Chemotherapy in First-line Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC) - daNIS-2

Start: Sep 2021Est. completion: Aug 2024511 patients
Phase 3Completed
NCT04329949Corcept TherapeuticsRelacorilant, 100 mg and 25 mg

Study of Relacorilant in Combination With Nab-Paclitaxel in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

Start: Jun 2020Est. completion: Mar 202243 patients
Phase 3Terminated
NCT02101021GSKMomelotinib

Gemcitabine and Nab-paclitaxel Combined With Momelotinib in Participants With Previously Untreated Metastatic Pancreatic Ductal Adenocarcinoma

Start: Jun 2014Est. completion: Apr 201725 patients
Phase 3Terminated

BXCL701 and Pembrolizumab in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

Start: Aug 2023Est. completion: Nov 202722 patients
Phase 2Active Not Recruiting
NCT04666740MSDPembrolizumab

A Study of Pembrolizumab and Olaparib for People With Metastatic Pancreatic Ductal Adenocarcinoma and Homologous Recombination Deficiency or Exceptional Treatment Response to Platinum-Based Therapy

Start: Dec 2020Est. completion: Jan 202763 patients
Phase 2Active Not Recruiting

Study of Efficacy and Safety of NIS793 (With and Without Spartalizumab) in Combination With SOC Chemotherapy in First-line Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC)

Start: Oct 2020Est. completion: May 2024164 patients
Phase 2Terminated

A Health Service Research Study to Investigate Survival of Metastatic Pancreatic Cancer Patients After Sequential Chemotherapy

Start: Jan 2018Est. completion: Sep 202167 patients
Phase 2Terminated

Ph1b/2 Study of PF-04136309 in Combination With Gem/Nab-P in First-line Metastatic Pancreatic Patients

Start: May 2016Est. completion: Oct 201722 patients
Phase 2Terminated
NCT04888312Alligator BioscienceCD40 agonist mitazalimab in combination with chemotherapy

Safety and Efficacy of Mitazalimab in Combination With Chemotherapy in Pancreatic Cancer Patients

Start: Sep 2021Est. completion: Jun 202694 patients
Phase 1/2Active Not Recruiting
NCT02583477AstraZenecaMEDI4736 in combination with nab-paclitaxel and gemcitabine

Phase Ib/II Study of MEDI4736 Evaluated in Different Combinations in Metastatic Pancreatic Ductal Carcinoma

Start: Mar 2016Est. completion: Jul 201823 patients
Phase 1/2Completed

MK2 Inhibitor in Combination With mFOLFIRINOX for Untreated Metastatic Pancreatic Ductal Adenocarcinoma

Start: Jun 2025Est. completion: May 203051 patients
Phase 1Recruiting
NCT04809766LonzaAutologous Mesothelin-specific TCR-T Cells

Mesothelin-Specific T-Cells (FH-TCR-Tᴍsʟɴ) for the Treatment of Metastatic Pancreatic Ductal Adenocarcinoma

Start: Dec 2021Est. completion: Jan 20259 patients
Phase 1Terminated

A Study of the Safety and Tolerance of CAN04 in Combination With FOLFIRINOX in Subjects With Metastatic Pancreatic Ductal Adenocarcinoma

Start: Jul 2021Est. completion: Jun 202325 patients
Phase 1Completed
NCT04581343SandozCanakinumab injection; spartalizumab, nab-paclitaxel, gemcitabine

A Phase 1B Study of Canakinumab, Spartalizumab, Nab-paclitaxel, and Gemcitabine in Metastatic Pancreatic Cancer (PC) Patients

Start: Nov 2020Est. completion: Feb 202310 patients
Phase 1Completed

A Study of Ozanimod in Pregnant Women With Ulcerative Colitis and Their Offspring

Start: Dec 2025Est. completion: Jun 20331,182 patients
N/ANot Yet Recruiting

A Study on the Safety of Deucravacitinib Exposure in Pregnant Women and Their Offspring

Start: Aug 2024Est. completion: Feb 2029833 patients
N/AActive Not Recruiting

A Study on the Safety of Ozanimod Exposure in Pregnant Women and Their Offspring

Start: Jul 2022Est. completion: Jun 20321,182 patients
N/ARecruiting

Related Jobs in Oncology

Phase Legend

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

Key Insights

2 late-stage (Phase 3) programs, potential near-term approvals
3 actively recruiting trials targeting 5,450 patients
17 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.