Skip to main content

Triple Negative Breast Neoplasms

Oncology
17
Pipeline Programs
9
Companies
13
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
2
3
7
0
5
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
969%
ADC
215%
Small Molecule
215%
+ 6 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

9 companies ranked by most advanced pipeline stage

Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
6 programs
1
1
2
2
PembrolizumabPhase 3Monoclonal Antibody
Sacituzumab tirumotecanPhase 3
PembrolizumabPhase 2Monoclonal Antibody
PembrolizumabPhase 2Monoclonal Antibody
ladiratuzumab vedotinPhase 1/2ADC
+1 more programs
MSD
MSDIreland - Ballydine
6 programs
1
1
2
2
PembrolizumabPhase 3Monoclonal Antibody1 trial
Sacituzumab tirumotecanPhase 31 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
ladiratuzumab vedotinPhase 1/2ADC1 trial
+1 more programs
Active Trials
NCT02622074Completed60Est. Nov 2019
NCT03310957Completed185Est. Sep 2024
NCT05485766Recruiting23Est. Sep 2028
+3 more trials
Sandoz
SandozAustria - Kundl
1 program
1
alpelisibPhase 3Small Molecule1 trial
Active Trials
NCT04251533Terminated137Est. Feb 2026
Prevail Therapeutics
1 program
1
AbemaciclibPhase 2Small Molecule1 trial
Active Trials
NCT06365788Recruiting53Est. Dec 2028
NeoImmuneTech
NeoImmuneTechMD - Rockville
1 program
1
DocetaxelPhase 21 trial
Active Trials
NCT02124902Terminated148Est. Dec 2021
Pfizer
PfizerNEW YORK, NY
1 program
1
PF-03084014Phase 21 trial
Active Trials
NCT02299635Terminated19Est. Jan 2016
Replimune
ReplimuneMA - Woburn
1 program
1
Atezolizumab + RP1Phase 1/21 trial
Active Trials
NCT06067061Terminated2Est. May 2025
CytoDyn
CytoDynVANCOUVER, WA
1 program
350 mg leronlimabPHASE_1_2Monoclonal Antibody1 trial
Active Trials
NCT03838367Terminated10Est. Sep 2022
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
Bintrafusp alfaPHASE_21 trial
Active Trials
NCT04489940Terminated11Est. Jul 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
MSDSacituzumab tirumotecan
Sandozalpelisib
MSDPembrolizumab
MSDPembrolizumab
Prevail TherapeuticsAbemaciclib
Merck & Co.Bintrafusp alfa
MSDPembrolizumab
PfizerPF-03084014
NeoImmuneTechDocetaxel
ReplimuneAtezolizumab + RP1
CytoDyn350 mg leronlimab
MSDladiratuzumab vedotin
MSDPembrolizumab

Clinical Trials (13)

Total enrollment: 3,284 patients across 13 trials

NCT06841354MSDSacituzumab tirumotecan

A Study of Sacituzumab Tirumotecan (Sac-TMT, MK-2870) as Monotherapy and in Combination With Pembrolizumab (MK-3475) in Participants With Triple-Negative Breast Cancer (MK-2870-011/TroFuse-011)

Start: Mar 2025Est. completion: May 20301,000 patients
Phase 3Recruiting

Study Assessing the Efficacy and Safety of Alpelisib + Nab-paclitaxel in Subjects With Advanced TNBC Who Carry Either a PIK3CA Mutation or Have PTEN Loss

Start: Jun 2020Est. completion: Feb 2026137 patients
Phase 3Terminated
NCT03036488MSDPembrolizumab

Study of Pembrolizumab (MK-3475) Plus Chemotherapy vs Placebo Plus Chemotherapy as Neoadjuvant Therapy and Pembrolizumab vs Placebo as Adjuvant Therapy in Participants With Triple Negative Breast Cancer (TNBC) (MK-3475-522/KEYNOTE-522)

Start: Mar 2017Est. completion: Oct 20251,174 patients
Phase 3Completed
NCT05485766MSDPembrolizumab

Novel Neoadjuvant and Adjuvant Strategy for Germline BRCA 1/2 Mutated Triple Negative Breast Cancer

Start: Jul 2024Est. completion: Sep 202823 patients
Phase 2Recruiting

Bicalutamide and Abemaciclib in Inoperable or Metastatic Androgen Receptor-positive Triple-negative Breast Cancer

Start: Apr 2024Est. completion: Dec 202853 patients
Phase 2Recruiting
NCT04489940Merck & Co.Bintrafusp alfa

Bintrafusp Alfa in High Mobility Group AT-Hook 2 (HMGA2) Expressing Triple Negative Breast Cancer

Start: Oct 2020Est. completion: Jul 202211 patients
Phase 2Terminated
NCT04191135MSDPembrolizumab

Study of Olaparib Plus Pembrolizumab Versus Chemotherapy Plus Pembrolizumab After Induction With First-Line Chemotherapy Plus Pembrolizumab in Triple Negative Breast Cancer (TNBC) (MK-7339-009/KEYLYNK-009)

Start: Dec 2019Est. completion: Nov 2025462 patients
Phase 2Completed

A Study Evaluating PF-03084014 In Patients With Advanced Breast Cancer With Or Without Notch Alterations

Start: Feb 2015Est. completion: Jan 201619 patients
Phase 2Terminated

Neoadjuvant Treatment of Triple Negative Breast Cancer Patients With Docetaxel and Carboplatin to Assess Anti-tumor Activity

Start: Jul 2014Est. completion: Dec 2021148 patients
Phase 2Terminated
NCT06067061ReplimuneAtezolizumab + RP1

"neoBREASTIM": Atezolizumab Plus RP1 Oncolytic Immunotherapy in the NeoAdjuvant Setting of Triple-Negative Breast Cancer

Start: Apr 2024Est. completion: May 20252 patients
Phase 1/2Terminated
NCT03838367CytoDyn350 mg leronlimab

Leronlimab (PRO 140) Combined With Carboplatin in Patients With Cytokine Chemokine Receptor 5 Positive (CCR5+) mTNBC

Start: Apr 2019Est. completion: Sep 202210 patients
Phase 1/2Terminated
NCT03310957MSDladiratuzumab vedotin

Safety and Efficacy of SGN-LIV1A Plus Pembrolizumab for Patients With Locally-Advanced or Metastatic Triple-Negative Breast Cancer

Start: Feb 2018Est. completion: Sep 2024185 patients
Phase 1/2Completed
NCT02622074MSDPembrolizumab

Safety and Efficacy Study of Pembrolizumab (MK-3475) in Combination With Chemotherapy as Neoadjuvant Treatment for Participants With Triple Negative Breast Cancer (TNBC) (MK-3475-173/KEYNOTE-173)

Start: Jan 2016Est. completion: Nov 201960 patients
Phase 1Completed

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
3 actively recruiting trials targeting 3,284 patients
Monoclonal Antibody is the dominant modality (69% of programs)
9 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.