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Recurrent Plasma Cell Myeloma

Oncology
5
Pipeline Programs
8
Companies
23
Clinical Trials
1 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
0
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
1100%
+ 9 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

8 companies ranked by most advanced pipeline stage

Oregon Therapeutics
Oregon TherapeuticsFrance - Paris
1 program
1
CarfilzomibPhase 2
Sandoz
SandozAustria - Kundl
1 program
1
Laboratory Biomarker AnalysisPhase 21 trial
Active Trials
NCT02086552Completed28Est. Aug 2021
Oncolytics Biotech
Oncolytics BiotechAB - Calgary
2 programs
2
BortezomibPhase 11 trial
CarfilzomibPhase 1
Active Trials
NCT02514382Completed14Est. Apr 2022
Utah Medical
Utah MedicalIreland - Dublin
1 program
1
CarfilzomibPhase 11 trial
Active Trials
NCT03605719Completed23Est. Oct 2022
Knight Therapeutics
Knight TherapeuticsQC - Montréal
2 programs
CyclophosphamidePHASE_11 trial
CarfilzomibPHASE_21 trial
Active Trials
NCT01689987Completed18
NCT04850599Active Not Recruiting5Est. Feb 2029
City Therapeutics
City TherapeuticsMA - Cambridge
1 program
Actinium Ac 225-DOTA-DaratumumabPHASE_1Monoclonal Antibody1 trial
Active Trials
NCT05363111RecruitingEst. Mar 2027
Novartis
NovartisBASEL, Switzerland
1 program
Laboratory Biomarker AnalysisPHASE_2
Bristol Myers Squibb
1 program
Laboratory Biomarker AnalysisPHASE_25 trials
Active Trials
NCT03457142Terminated15Est. Nov 2024
NCT03425461Terminated6Est. Mar 2021
NCT03502577Terminated19Est. Apr 2022
+2 more trials

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
Knight TherapeuticsCarfilzomib
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
SandozLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis
City TherapeuticsActinium Ac 225-DOTA-Daratumumab
Utah MedicalCarfilzomib
Bristol Myers SquibbLaboratory Biomarker Analysis
Bristol Myers SquibbLaboratory Biomarker Analysis

Showing 15 of 23 trials with date data

Clinical Trials (23)

Total enrollment: 492 patients across 23 trials

Isatuximab, Carfilzomib, and Pomalidomide for the Treatment of Relapsed or Refractory Multiple Myeloma

Start: Jun 2022Est. completion: Feb 20295 patients
Phase 2Active Not Recruiting
NCT03457142Bristol Myers SquibbLaboratory Biomarker Analysis

Abatacept, Ixazomib Citrate, and Dexamethasone in Treating Patients With Multiple Myeloma Resistant to Chemotherapy

Start: Sep 2018Est. completion: Nov 202415 patients
Phase 2Terminated
NCT03333746Bristol Myers SquibbLaboratory Biomarker Analysis

Lenalidomide and Nivolumab in Treating Patients With Relapsed or Refractory Multiple Myeloma

Start: Mar 2018Est. completion: Nov 20181 patients
Phase 2Terminated
NCT03252600Bristol Myers SquibbLaboratory Biomarker Analysis

Lenalidomide, Dexamethasone, and Elotuzumab With or Without Cyclophosphamide in Treating Patients With Relapsed Primary Amyloidosis

Start: Aug 2017Est. completion: Dec 202353 patients
Phase 2Unknown
NCT03146650Bristol Myers SquibbLaboratory Biomarker Analysis

Nivolumab and Ipilimumab in Treating Patients With Metastatic/Recurrent ACC of All Sites and Non-ACC Salivary Gland Cancer

Start: May 2017Est. completion: Aug 202525 patients
Phase 2Unknown
NCT02232516Bristol Myers SquibbLaboratory Biomarker Analysis

Romidepsin and Lenalidomide in Treating Patients With Previously Untreated Peripheral T-Cell Lymphoma

Start: Jun 2015Est. completion: Aug 202430 patients
Phase 2Unknown
NCT02086552SandozLaboratory Biomarker Analysis

Sonidegib and Lenalidomide After Stem Cell Transplant in Treating Patients With Multiple Myeloma

Start: Jan 2014Est. completion: Aug 202128 patients
Phase 2Completed
NCT01620190Bristol Myers SquibbLaboratory Biomarker Analysis

Paclitaxel Albumin-Stabilized Nanoparticle Formulation in Treating Patients With Previously Treated Advanced Non-small Cell Lung Cancer

Start: Dec 2012Est. completion: Apr 201926 patients
Phase 2Completed
NCT01518465Bristol Myers SquibbLaboratory Biomarker Analysis

Dalteparin, Lenalidomide, and Low-Dose Dexamethasone in Treating Patients With Previously Untreated Multiple Myeloma

Start: Jan 2012Est. completion: Oct 201713 patients
Phase 2Terminated
NCT01083706Bristol Myers SquibbLaboratory Biomarker Analysis

Azacitidine in Treating Patients With Relapsed Myelodysplastic Syndrome, Chronic Myelomonocytic Leukemia, or Acute Myeloid Leukemia Who Have Undergone Stem Cell Transplant

Start: Apr 201043 patients
Phase 2Completed
NCT03015896Bristol Myers SquibbLaboratory Biomarker Analysis

Nivolumab and Lenalidomide in Treating Patients With Relapsed or Refractory Non-Hodgkin or Hodgkin Lymphoma

Start: Feb 2017Est. completion: Dec 202636 patients
Phase 1/2Active Not Recruiting
NCT05363111City TherapeuticsActinium Ac 225-DOTA-Daratumumab

Radioimmunotherapy (111Indium/225Actinium-DOTA-daratumumab) for the Treatment of Relapsed/Refractory Multiple Myeloma

Start: Nov 2022Est. completion: Mar 2027
Phase 1Recruiting

Dexamethasone, Carfilzomib, & Nivolumab With Pelareorep for Relapsed/Refractory Multiple Myeloma

Start: Oct 2018Est. completion: Oct 202223 patients
Phase 1Completed
NCT03425461Bristol Myers SquibbLaboratory Biomarker Analysis

Anti-SEMA4D Monoclonal Antibody VX15/2503 With Nivolumab or Ipilimumab in Treating Patients With Stage III or IV Melanoma

Start: Jun 2018Est. completion: Mar 20216 patients
Phase 1Terminated
NCT03502577Bristol Myers SquibbLaboratory Biomarker Analysis

BCMA-Specific CAR T-Cells Combined With a Gamma Secretase Inhibitor (JSMD194) to Treat Relapsed or Persistent Multiple Myeloma

Start: May 2018Est. completion: Apr 202219 patients
Phase 1Terminated
NCT03576612Bristol Myers SquibbLaboratory Biomarker Analysis

GMCI, Nivolumab, and Radiation Therapy in Treating Patients With Newly Diagnosed High-Grade Gliomas

Start: Feb 2018Est. completion: Jun 202341 patients
Phase 1Completed
NCT03103971Bristol Myers SquibbLaboratory Biomarker Analysis

huJCAR014 CAR-T Cells in Treating Adult Patients With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma or Acute Lymphoblastic Leukemia

Start: Nov 2017Est. completion: Mar 202455 patients
Phase 1Terminated
NCT03061188Bristol Myers SquibbLaboratory Biomarker Analysis

Phase I/Ib Study of Nivolumab & Veliparib in Patients With Advanced Solid Tumors & Lymphoma

Start: May 2017Est. completion: Aug 202015 patients
Phase 1Completed
NCT02334865Bristol Myers SquibbLaboratory Biomarker Analysis

SVN53-67/M57-KLH Peptide Vaccine in Treating Patients With Newly Diagnosed Multiple Myeloma Receiving Lenalidomide Maintenance Therapy

Start: Apr 2017Est. completion: May 202618 patients
Phase 1Active Not Recruiting

Wild-Type Reovirus, Bortezomib, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma

Start: Aug 2015Est. completion: Apr 202214 patients
Phase 1Completed

Hydroxychloroquine, Cyclophosphamide, Dexamethasone, and Sirolimus in Treating Patients With Relapsed or Refractory Multiple Myeloma

Start: Sep 201218 patients
Phase 1Completed
NCT02414100Bristol Myers SquibbLaboratory Biomarker Analysis

Patient Derived Cancer Cell Lines in Identifying Molecular Changes in Patients With Previously Untreated Pancreatic Cancer Receiving Gemcitabine Hydrochloride-Based Chemotherapy

Start: Dec 2013Est. completion: Dec 20160
N/AWithdrawn
NCT01649791Bristol Myers SquibbLaboratory Biomarker Analysis

Lenalidomide as Chemoprevention in Treating Patients With High-Risk, Early-Stage B-Cell Chronic Lymphocytic Leukemia

Start: Jan 2010Est. completion: Oct 20148 patients
N/ATerminated

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 actively recruiting trials targeting 492 patients
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.