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Exudative Age-related Macular Degeneration

Ophthalmology
10
Pipeline Programs
4
Companies
10
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
0
1
7
0
0
2
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
2100%
+ 9 programs with unclassified modality

Ophthalmology is a $3.7B market with a mature, consolidating portfolio dominated by glaucoma treatments and emerging corneal/retinal therapies.

$3.7B marketMature→ Stable30 products15 companies

Key Trends

  • Glaucoma therapeutics (prostaglandin analogs, adrenergic agents) represent 60%+ of spending but face patent cliffs 2028-2034
  • Innovative mechanisms (NGF agonists, LFA-1 antagonists, RTKIs) gaining traction in dry eye and retinal disease segments
  • Heavy trial activity (2,656 total) skewed toward Phase 4 (369) and Phase 3 (442), indicating mature clinical development landscape

Career Verdict

Ophthalmology offers stable mid-career opportunities with strong Commercial and Medical Affairs salaries, but limited innovation catalysts and significant patent cliff risk warrant careful timing of entry.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1LUMIGANDeclining
$697M
AbbVie·LOE_APPROACHING
#2OXERVATEStable
$493M
Unspecified·PEAK
#3XIIDRAStable
$473M
Bausch + Lomb·PEAK7.6yr
#4INLYTAGrowing
$467M
Pfizer·PEAK11.2yr
#5HUMIRADeclining
$258M
AbbVie·LOE_APPROACHING

Drug Class Breakdown

Prostaglandin Analogs (Bimatoprost)
$697M(19%)

mature, losing exclusivity

Nerve Growth Factor Agonists
$493M(13%)

peak growth in corneal disease

LFA-1 Antagonists (Dry Eye)
$473M(13%)

sustained peak sales

Receptor Tyrosine Kinase Inhibitors
$467M(13%)

expanding in retinal indications

Alpha-2 Adrenergic Agonists
$362M(10%)

mature, multiple LOE approaching

Combination Therapies (Brimonidine/Timolol)
$232M(6%)

mature, losing exclusivity

Complement Inhibitors
$223M(6%)

mature immunology approach

Career Outlook

Stable

Ophthalmology offers predictable mid-career growth with strong Commercial ($158K) and Medical Affairs ($247K) compensation but faces structural headwinds: patent cliffs 2028-2034 eliminate $97M in revenue, glaucoma franchise maturity limits blockbuster potential, and modest trial volume (2,656) signals incremental R&D expansion. Best suited for professionals seeking stable roles in established therapeutic areas rather than disruptive innovation.

Breaking In

Enter via Clinical Operations or Commercial analyst roles at CROs (Syneos 210 jobs) or large diagnostics players (Labcorp 904) to build domain expertise before targeting pharma MSL/Medical Affairs positions.

For Experienced Professionals

Experienced professionals should prioritize Medical Affairs and Market Access roles leveraging mature market knowledge; avoid product-specific expertise in glaucoma due to patent cliff concentration, and consider adjacent areas (retinal, corneal) where innovation catalysts remain.

In-Demand Skills

Glaucoma/dry eye clinical expertise and key opinion leader relationshipsRegulatory navigation for mature small-molecule formulations and device combinationsMarket access and reimbursement strategy (high generic/biosimilar pressure)

Best For

Medical Science Liaison (MSL) — strong $247K average salary, KOL interface criticalCommercial/Brand Manager — competitive $158K salaries, established product lifecycle managementClinical Operations Manager — high hiring volume (409 jobs), trial coordination in Phase 4-heavy pipeline

Hiring Landscape

$59K-$247K

Ophthalmology hiring (3,202 jobs) is distributed across diagnostics/devices (Labcorp 904, Abbott 348) and pharma commercial functions rather than concentrated in R&D. Top pharmaceutical employers (Pfizer 60, AstraZeneca 100, Regeneron 168) show modest pharma-specific headcount relative to market size, suggesting outsourced CRO and distributor dependency. Medical Affairs ($247K avg salary) commands premium compensation, signaling high barrier to entry but strong mid-career upside.

3,202
Open Roles
5
Companies Hiring
5
Departments

Top Hiring Companies

904Growing
348Stable
168Growing
219Stable

By Department

Clinical Operations(13%)
$150K
Commercial(10%)
$158K
Medical Affairs(3%)
$247K
R&D(6%)
$145K
Engineering(9%)
$112K

Clinical Operations and Commercial roles offer entry-level stability ($150K-$158K); Medical Affairs commands premium salaries ($247K) but requires advanced credentials; limited R&D hiring (207 jobs) suggests constrained innovation investment.

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Sandoz
SandozAustria - Kundl
3 programs
1
2
ranibizumabPhase 4Monoclonal Antibody1 trial
ranibizumabPhase 4Monoclonal Antibody1 trial
LHA510 ophthalmic suspensionPhase 21 trial
Active Trials
NCT02355028Completed136Est. Oct 2016
NCT02976194Unknown28Est. Jan 2020
NCT01810042Completed49Est. Feb 2013
Alcon
AlconFORT WORTH, TX
5 programs
1
4
AL-78898APhase 21 trial
ESBA1008 solutionPhase 21 trial
ESBA1008 solutionPhase 21 trial
LHA510 ophthalmic suspensionPhase 2
ESBA1008 solutionPhase 1/21 trial
Active Trials
NCT01304693Completed376Est. Mar 2013
NCT01157065Completed99Est. Apr 2012
NCT01849692Completed107Est. Jan 2015
+1 more trials
Ribomic
RibomicJapan - Tokyo
2 programs
2
RBM-007Phase 21 trial
RBM-007 Injectable SolutionPhase 21 trial
Active Trials
NCT04640272Completed40Est. Dec 2021
NCT04200248Completed94Est. Dec 2021
Innovation Pharmaceuticals
1 program
Aflibercept 8mgN/A1 trial
Active Trials
NCT07340372Not Yet Recruiting80Est. Dec 2027

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
Sandozranibizumab
Sandozranibizumab
RibomicRBM-007
RibomicRBM-007 Injectable Solution
SandozLHA510 ophthalmic suspension
AlconESBA1008 solution
AlconESBA1008 solution
AlconAL-78898A
AlconESBA1008 solution
Innovation PharmaceuticalsAflibercept 8mg

Clinical Trials (10)

Total enrollment: 1,182 patients across 10 trials

Intraocular Cytokine in Recurrence of Polypoidal Choroidal Vasculopathy

Start: Nov 2016Est. completion: Jan 202028 patients
Phase 4Unknown

Indocyanine Angiographic Changes of Choroidal Neovascularization by Ranibizumab

Start: Oct 2010Est. completion: Feb 201349 patients
Phase 4Completed

A Multi-Center, Open Label, Extension Study Assessing the Efficacy and Safety of Additional Intravitreal Injections of RBM-007 in Subjects With Wet Age-related Macular Degeneration

Start: Nov 2020Est. completion: Dec 202140 patients
Phase 2Completed
NCT04200248RibomicRBM-007 Injectable Solution

A Phase II Study of RBM-007 Alone and RBM-007 With Eylea® in Subjects With Wet Age-related Macular Degeneration

Start: Dec 2019Est. completion: Dec 202194 patients
Phase 2Completed
NCT02355028SandozLHA510 ophthalmic suspension

LHA510 Proof-of-Concept Study as a Maintenance Therapy for Patients With Wet Age-Related Macular Degeneration

Start: Mar 2015Est. completion: Oct 2016136 patients
Phase 2Completed
NCT01849692AlconESBA1008 solution

ESBA1008 Microvolume Study

Start: Jun 2013Est. completion: Jan 2015107 patients
Phase 2Completed
NCT01796964AlconESBA1008 solution

Efficacy and Safety Study of ESBA1008 Versus EYLEA®

Start: Mar 2013Est. completion: Aug 2014173 patients
Phase 2Completed

Evaluation of AL-78898A in Exudative Age-Related Macular Degeneration

Start: Jun 2011Est. completion: Apr 201299 patients
Phase 2Completed
NCT01304693AlconESBA1008 solution

ESBA1008 Safety, Tolerability and Effects in Wet Age-Related Macular Degeneration (AMD) Patients

Start: Oct 2010Est. completion: Mar 2013376 patients
Phase 1/2Completed

Home Monitoring in eAMD Treatment

Start: Mar 2026Est. completion: Dec 202780 patients
N/ANot Yet Recruiting

Related Jobs in Ophthalmology

Phase Legend

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

Key Insights

4 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.