pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Drugs
by stage
  • Marketed
  • Phase 3
  • Phase 2
  • Phase 1
  • Preclinical
browse
  • Most catalysts
  • Recently active
  • All drugs →
  • Companies
  • Patent cliff
Calendar
what
  • Trial readouts
  • PDUFA dates
  • Approvals
  • Earnings
when
  • Upcoming
  • Month grid
  • Recently passed
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
  • Drugs
  • Calendar
  • Companies
Hubs
  • Topics
  • Patent cliff
  • Publications
  • Readouts
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search
  1. pharmadog
  2. ›drugs
  3. ›Voxzogo
drug · protein
save

vosoritide

Marketedupdated 5mo ago
by $BMRN BIOMARIN PHARMACEUTICAL INC🔗 ChEMBL
Approved
community read0 votes

Protein drug with a maximum clinical stage of Approval (across all indications), with an approval for achondroplasia and bone disease and 2 investigational indications.

targets

Atrial natriuretic peptide receptor 2

all catalysts(0)

nothing on the calendar yet

Trials studying vosoritide

  • phase3Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasiarecruitingn=160
  • phase2A Study of Vosoritide in Children With Noonan Syndrome With Inadequate Growth During or After Human Growth Hormone Treatmentrecruitingn=30
  • phase2A Study of Vosoritide Versus Placebo in Children With Hypochondroplasia Aged 0 to < 36 Monthsrecruitingn=60
  • phase2A Clinical Trial to Evaluate Safety of Vosoritide in At-risk Infants With Achondroplasiaactive not recruitingn=20
  • phase2A Phase 2 Study of Vosoritide in Children With Idiopathic Short Staturerecruitingn=100
  • phase3Interventional Study of Vosoritide for the Treatment of Children With Hypochondroplasiaactive not recruitingn=80
  • phase3Long-Term Extension Study of Vosoritide to Treat Children With Hypochondroplasiaenrolling by invitationn=140

Patent cliff

source: FDA Orange Book
first barrier falls
Oct 20, 2026
21 days

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (24)

  • Jul 11, 2042method-of-use (U-3927)US 12233106
  • Jul 11, 2042method-of-use (U-3927)US 12233106
  • Jul 11, 2042method-of-use (U-3927)US 12233106
  • Aug 1, 2036formulationUS 10646550
  • Aug 1, 2036formulationUS 10646550
  • Aug 1, 2036formulationUS 10646550
  • Aug 1, 2036formulationUS 11590204
  • Aug 1, 2036formulationUS 11590204
  • Aug 1, 2036formulationUS 11590204
  • Aug 1, 2036method-of-use (U-3927)US 11911446
  • Aug 1, 2036method-of-use (U-3927)US 11911446
  • Aug 1, 2036method-of-use (U-3927)US 11911446
  • Aug 1, 2036formulationUS 12514906
  • Aug 1, 2036formulationUS 12514906
  • Aug 1, 2036formulationUS 12514906
  • Aug 1, 2036formulationUS 9907834
  • Aug 1, 2036formulationUS 9907834
  • Aug 1, 2036formulationUS 9907834
  • Jun 11, 2030compositionUS 81982423.7y
  • Jun 11, 2030compositionUS 81982423.7y
  • Jun 11, 2030compositionUS 81982423.7y
  • May 20, 2030method-of-use (U-3927)US RE482673.6y
  • May 20, 2030method-of-use (U-3927)US RE482673.6y
  • May 20, 2030method-of-use (U-3927)US RE482673.6y

FDA exclusivities (12)

  • Oct 20, 2030ODE-449Orphan Drug (7y)4.1y
  • Oct 20, 2030ODE-449Orphan Drug (7y)4.1y
  • Oct 20, 2030ODE-449Orphan Drug (7y)4.1y
  • Nov 19, 2028ODE-387Orphan Drug (7y)2.1y
  • Nov 19, 2028ODE-387Orphan Drug (7y)2.1y
  • Nov 19, 2028ODE-387Orphan Drug (7y)2.1y
  • Nov 19, 2026NCENew Chemical Entity (5y)51d
  • Nov 19, 2026NCENew Chemical Entity (5y)51d
  • Nov 19, 2026NCENew Chemical Entity (5y)51d
  • Oct 20, 2026NPPNew Product (3y)21d
  • Oct 20, 2026NPPNew Product (3y)21d
  • Oct 20, 2026NPPNew Product (3y)21d

News(8)

  • 5 biotechs braving the commercial waters with product launches
    A growing number of biotechs are entering the market with newly launched medicines, a pattern indicative of “improving capital markets,” according to Jefferies’ Andrew Tsai.
    biospace · 13d ago
  • Teva claims success in celiac study; BioMarin, Ascendis settle patent dispute
    Teva believes the therapy has “pipeline-in-a-product” potential. Elsewhere, a high-stakes trial was paused and GSK advanced a competitor to Moderna’s flu shot.
    biopharma_dive · 26d ago
  • Biomarin nabs big royalties in achondroplasia patent settlement with Ascendis
    Biomarin has granted Ascendis a non-exclusive, worldwide license to use navepegritide, the active ingredient in the latter company’s recently approved achondroplasia drug Yuviwel, in exchange for 1…
    biospace · 28d ago
  • BioMarin acquires experimental drug for rare bone disorder in $275M deal
    The Alesta buyout helps restock BioMarin's pipeline with an asset it says could “reach our largest addressable patient population,” joining other muscle and skeletal disease treatments in development.
    biopharma_dive · 1mo ago
  • BioMarin bulks up bone unit with $275M Alesta buyout to challenge AstraZeneca
    BioMarin Pharmaceutical has agreed to buy Alesta Therapeutics for $275 million upfront, positioning the biopharma to challenge AstraZeneca in the rare bone disease market.
    fiercebiotech · 1mo ago
  • Silence cashes in on ‘differentiated’ data; UK reaffirms support for childhood vaccines
    Some analysts believe Silence’s polycythemia vera drug could be superior to a closely watched Takeda medicine. Elsewhere, the FDA spurned a radiopharmaceutical and AbCellera shares climbed to level…
    biopharma_dive · 1mo ago
  • BioMarin axes asset from $270M Inozyme takeover, ending run in rare metabolic indication
    BioMarin’s discontinued drug showed biomarker benefits in a Phase 3 study for ENPP1 deficiency but these failed to translate to clinical improvements.
    biospace · 1mo ago
  • BioMarin drug acquired in buyout misses goal in rare disease study
    Tested in a condition known as ENPP1 deficiency, the treatment failed a trial goal that’s important to regulators, spurring doubts about its approval prospects.
    biopharma_dive · 4mo ago
brand
Voxzogo
trade names
Voxzogo
generic
vosoritide
MOA
Atrial natriuretic peptide receptor B binding agent
indication
Noonan Syndrome
phase
marketed
Data sources
ClinicalTrials.gov · OpenTargets
last refreshed 1h ago
Found something off?
🐶 something off?

Report a data issue

Tell Bork what looks wrong — wrong sponsor, stale phase, mislinked ticker, anything. We’ll triage and fix.

comments(0)

5-min edit window · permanent after that
sign in to leave a comment · permanent archive after 5 minutes
no comments yet — first sniff?