PureTech
9
0
1
5
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
High Risk
Score: 75/100
22.2%
2 terminated/withdrawn out of 9 trials
71.4%
-15.1% vs industry average
11%
1 trials in Phase 3/4
20%
1 of 5 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (9)
A Phase 1 Study With LYT-200 in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AML), or With Relapsed/Refractory, High-risk Myelodysplastic Syndrome (MDS)
Role: lead
PK of Deupirfenidone Versus Pirfenidone in Older Healthy Subjects
Role: lead
Study to Determine Potential for Drug-drug Interactions When Co-administering Deupirfenidone (LYT-100) and Nintedanib
Role: lead
Trial to Evaluate the Efficacy and Safety of LYT-100 (Deupirfenidone) Compared to Pirfenidone in Adults With Idiopathic Pulmonary Fibrosis (IPF)
Role: lead
LYT-100 in Patients With Idiopathic Pulmonary Fibrosis (IPF)
Role: lead
LYT-200 Alone and in Combination With Chemotherapy or Tislelizumab in Patients With Locally Advanced or Metastatic Solid Tumors
Role: lead
LYT-100 in Patients With BCRL
Role: lead
LYT-100 in Post-acute COVID-19 Respiratory Disease
Role: lead
LYT-300 in Healthy Volunteers
Role: lead
All 9 trials loaded