Debiopharm has started enrolling patients in its CATRIPCA Phase I clinical trial evaluating Debio 1143 in combination with Merck’s Keytruda for the treatment of cancer.
Debio 1143 is an investigational, oral inhibitor of apoptosis proteins (IAP) antagonist that stimulates programmed cell death and anti-tumour immunity, while Keytruda is an anti-PD1 drug.
Go deeper with GlobalData
Discover B2B Marketing That Performs
Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.
The Phase I trial will investigate the combination therapy’s safety and preliminary efficacy in people with non-microsatellite instability (non-MSI)-high colorectal cancer (CRC) and pancreatic ductal adenocarcinoma cancer (PDAC).
It focuses on two cancers that have intrinsic resistance to immune checkpoint inhibitors (ICI).
Around 46 patients who do not have other available therapeutic options will be enrolled in the dose-escalation and expansion parts of the trial.
The study extension’s primary endpoint is the objective response rate.
US Tariffs are shifting - will you react or anticipate?
Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.
By GlobalDataDebiopharm chief development officer Dr Angela Zubel said: “This study is the third of a series of immuno-oncology studies investigating the effect of Debio 1143 in combination with ICIs.
“The study will evaluate a particularly difficult patient population, primarily in the immune-refractory setting with hopes that the Debio 1143-pembrolizumab combination will open up new possibilities for these patients.”
In a separate development, Keytruda is being investigated in combination with Oncologie’s bavituximab in a Phase II trial involving advanced gastric or gastroesophageal cancer patients.
Bavituximab is an investigational monoclonal antibody that blocks phosphatidylserine (PS) activation of various immune cell receptors.
The global, multi-centre, open-label, single-arm Phase II study will assess the safety, tolerability, and efficacy of the combination in about 80 patients across the US, UK, South Korea and Taiwan.
Patient enrolment has started for the trial.
