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Advanced Cholangiocarcinoma

Oncology
10
Pipeline Programs
12
Companies
9
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
1
5
0
4
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
563%
Monoclonal Antibody
338%
+ 11 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

12 companies ranked by most advanced pipeline stage

Taiho Pharma
Taiho PharmaJapan - Tokyo
3 programs
1
1
FutibatinibPhase 3Small Molecule
TAS-120Phase 2
TAS-120N/A
QED Therapeutics
QED TherapeuticsCA - Palo Alto
2 programs
1
1
BGJ398Phase 3
BGJ398Phase 2
Helsinn
HelsinnIreland - Dublin
2 programs
1
1
BGJ398Phase 3
BGJ398Phase 2
Servier
ServierFrance - Suresnes
1 program
1
AG-120Phase 31 trial
Active Trials
NCT02989857Completed187Est. May 2021
MSD
MSDIreland - Ballydine
1 program
1
PembrolizumabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT02982720Terminated4Est. Feb 2018
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
PembrolizumabPhase 2Monoclonal Antibody
Incyte
IncyteDE - Wilmington
1 program
1
PemigatinibPhase 1/2Small Molecule
Taiho Oncology
Taiho OncologyNJ - Princeton
3 programs
TAS-120N/A1 trial
TAS-120PHASE_21 trial
FutibatinibPHASE_3Small Molecule1 trial
Active Trials
NCT04507503Approved For Marketing
NCT05727176Recruiting120Est. Dec 2026
NCT04093362Terminated10Est. Apr 2024
BridgeBio Pharma
BridgeBio PharmaCA - Palo Alto
2 programs
BGJ398PHASE_21 trial
BGJ398PHASE_31 trial
Active Trials
NCT02150967Terminated143Est. Feb 2022
NCT03773302Terminated48Est. Mar 2023
Chia Tai TianQing Pharmaceutical Group
1 program
AnlotinibPHASE_1_2Small Molecule1 trial
Active Trials
NCT03996408Unknown42Est. Mar 2022
Genentech
GenentechCA - Oceanside
1 program
PemigatinibPHASE_1_2Small Molecule1 trial
Active Trials
NCT06439485Recruiting25Est. Feb 2030
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
Taiho OncologyFutibatinib
BridgeBio PharmaBGJ398
ServierAG-120
Taiho OncologyTAS-120
MSDPembrolizumab
BridgeBio PharmaBGJ398
GenentechPemigatinib
Chia Tai TianQing Pharmaceutical GroupAnlotinib

Clinical Trials (9)

Total enrollment: 579 patients across 9 trials

Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements

Start: Jan 2021Est. completion: Apr 202410 patients
Phase 3Terminated

Phase 3 Study of BGJ398 (Oral Infigratinib) in First Line Cholangiocarcinoma With FGFR2 Gene Fusions/Translocations

Start: Dec 2019Est. completion: Mar 202348 patients
Phase 3Terminated

Study of AG-120 in Previously Treated Advanced Cholangiocarcinoma With IDH1 Mutations (ClarIDHy)

Start: Feb 2017Est. completion: May 2021187 patients
Phase 3Completed

Study of Futibatinib in Patients With Advanced Cholangiocarcinoma With FGFR2 Fusion or Rearrangement

Start: Jul 2023Est. completion: Dec 2026120 patients
Phase 2Recruiting
NCT02982720MSDPembrolizumab

Evaluating Combination Immunotherapy for Advanced Cholangiocarcinoma With Pembrolizumab and PEG-Intron

Start: Jul 2017Est. completion: Feb 20184 patients
Phase 2Terminated

A Phase II, Single Arm Study of BGJ398 in Patients With Advanced Cholangiocarcinoma

Start: Jul 2014Est. completion: Feb 2022143 patients
Phase 2Terminated

Phase I/II Trial of Pemigatinib in Combination With Atezolizumab and Bevacizumab for Treatment of Advanced Cholangiocarcinoma With FGFR2 Fusion

Start: Nov 2024Est. completion: Feb 203025 patients
Phase 1/2Recruiting

Study of TQB2450 Combined With Anlotinib in Subjects With Advanced Cholangiocarcinoma

Start: Jun 2019Est. completion: Mar 202242 patients
Phase 1/2Unknown

Expanded Access Study of TAS-120 in Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements

N/AApproved For Marketing

Related Jobs in Oncology

Phase Legend

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

Key Insights

4 late-stage (Phase 3) programs, potential near-term approvals
2 actively recruiting trials targeting 579 patients
12 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.