Registry-listed formulations

Nadunolimab · chembl:CHEMBL5095365

Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.

2 source entries across 2 studies. This list may not include all unresolved or historical entries.

  • CAN04Registry intervention

    Linked study entry; product equivalence not established

    View study and source
  • CAN04Registry product

    Named ingredient; product remains distinct

    Formulation reported by source: SOLUTION FOR INFUSION

    Named ingredient; exact form unconfirmed. This mention does not add to the molecule trial count.

    View study and source

Success Metrics

Clinical Success Rate
100.0%

Based on 2 completed trials

Completion Rate
100%(2/2)
Active Trials
3(60%)
Results Posted
0%(0 trials)

Phase Distribution

Phase 1
1
20%
Phase 1/2
3
60%
Phase 2
1
20%

Phase Distribution

1

Early Stage

4

Mid Stage

0

Late Stage

Phase Distribution5 total trials
Phase 1Safety & dosage
1(20.0%)
Phase 1/2Combined phases
3(60.0%)
Phase 2Efficacy & side effects
1(20.0%)

Highest Phase Reached

Phase 2

Trial Status & Enrollment

Completion Rate

100.0%

2 of 2 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

3

trials recruiting

Total Trials

5

all time

Status Distribution
Active(3)
Completed(2)

Detailed Status

Recruiting3
Completed2

Development Timeline

Analytics

Development Status

Total Trials
5
Active
3
Success Rate
100.0%
Most Advanced
Phase 1/2

Trials by Phase

Phase 11 (20.0%)
Phase 1/23 (60.0%)
Phase 21 (20.0%)

Trials by Status

completed240%
recruiting360%

Recent Activity

Clinical Trials (5)

Drug Details

Intervention Type
Varies by study
Molecule Type
Antibody
Total Trials
5

External References