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About 20S proteasome

The 20S proteasome is a core component of the ubiquitin-proteasome system (UPS), responsible for degrading damaged or misfolded proteins to maintain cellular homeostasis. As a barrel-shaped structure, it plays a vital role in protein turnover within cells.

1
Approved Drugs
1
Companies
1
Indications
1
Therapeutic Areas
Broadest Approval
KYPROLIS
ONYX PHARMS AMGEN
1
approved indications

Top 20S proteasome Drugs

KYPROLIS
ONYX PHARMS AMGEN
1 indications · 2012
🏢

ONYX PHARMS AMGEN is the only company with an approved drug targeting the 20S proteasome.

20S proteasome Drug Modality Landscape

Modalities

Small molecule
1
100%

Routes of Administration

💉 IV
1
100%
💡

Only one approved drug targets 20S proteasome, using small molecule modality.

The lack of diverse modalities represents a whitespace opportunity for novel approaches like antibodies or PROTACs.

Small molecules only

20S proteasome Clinical Trials 215 trials

Phase 1-4 trials started in 2008 or later that test an FDA-approved drug acting on 20S proteasome. Source: ClinicalTrials.gov. How we count

215
Total Trials
83
Active
96
Completed
73%
Completion Rate

Completion by Phase

Phase Total Completed Stopped Active Completion
Phase 1 98 55 18 24 75%
Phase 2 83 29 15 39 66%
Phase 3 30 10 2 18 83%
Phase 4 4 2 0 2 100%

Top Sponsors

Amgen 21 95%
National Cancer Institute (N... 11 60%
M.D. Anderson Cancer Center 9 56%
University of Chicago 8 100%
Mayo Clinic 6 50%
Janssen Research & Developme... 6 67%
Memorial Sloan Kettering Can... 5 100%
Hackensack Meridian Health 5 100%

By Modality

Small molecule
215 73%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Phase 3 Readout Calendar Pro

7 Phase 3 trials testing approved 20S proteasome drugs across all sponsors.

Full calendar →
Q2 2027
bb2121
Celgene · Multiple Myeloma
Estimated · stale NCT03651128
Q4 2027
BMS-986393
Juno Therapeutics, Inc., a Bristol-Myers Squibb Company · Relapsed or Refractory Multiple Myeloma (RRMM)
Estimated · aging NCT06615479
Q4 2027
Etentamig
AbbVie · Multiple Myeloma
Estimated · aging NCT06158841
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Coverage: trials whose intervention is an approved drug targeting 20S proteasome. Pre-approval candidates with development codes (e.g. AZD0901, MK-7240) are not yet linked. Anchored on CT.gov primary completion date.

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Competitive Landscape

  • • 1 companies competing
  • • Market share by company

Full Drug Portfolio

  • • All 1 approved drugs
  • • Approval dates & indications

Genetic Validation

  • • Full genetic evidence table
  • • Effect sizes & directions

Approval Timeline

  • • Full 1-drug timeline
  • • First-of-modality markers

Clinical Trials Analysis

  • • Sponsors: 103 (27 companies)
  • • Completion rates by condition
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Full summary • All drugs • Genetic evidence • Trials • Timeline

How We Count Trials

  • Trials: phase 1-4 interventional trials on ClinicalTrials.gov that started in 2008 or later and test an FDA-approved drug acting on 20S proteasome. A trial counts if an approved drug acting on 20S proteasome is in any arm, including as a comparator, and a trial that tests two such drugs counts once. Trials that test only unapproved drugs are not counted. A trial listed as phase 1/2 counts as phase 1, and phase 2/3 as phase 2.
  • Active: recruiting, not yet recruiting, enrolling by invitation, or active and no longer recruiting.
  • Completion rate: of the trials that have ended, the share marked Completed rather than Terminated or Withdrawn. Completed means the trial ended as planned; it does not mean the drug worked. Suspended trials are not counted as ended.
  • Stopped: terminated or withdrawn. Trials stop for many reasons, including slow enrolment and business decisions, not only safety or efficacy.
  • Sponsors: the lead sponsor of each trial. Companies are the sponsors ClinicalTrials.gov classes as industry; the rest are universities, hospitals, cooperative groups, government bodies and individuals.