Certepetide Phase 1b/2a Continuous Infusion Trial in mPDAC
Stopped: Management Decision
0Started 2030-01
Plain-language summary
The goal of this clinical trial is to test a new drug plus standard treatment compared with standard treatment alone in people with metastatic pancreatic ductal adenocarcinoma.
The main questions it aims to answer are:
* is the new drug plus standard treatment safe and tolerable
* is the new drug plus standard treatment more effective than standard treatment
Participants will:
* Visit the clinic three times every 28 days for treatment and tests
* Have CT or MRI scans every 8 weeks while on treatment
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Histologically or cytologically confirmed metastatic pancreatic ductal adenocarcinoma that has not been treated previously and be eligible for treatment with nab-paclitaxel and gemcitabine
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
* Life expectancy ≥ 3 months
* At least one measurable tumor lesion as assessed by RECIST 1.1
* Adequate organ and marrow function
* Adequate contraception
Exclusion Criteria:
* Concurrent use of any other anti-cancer therapy including chemotherapy, targeted therapy, immunotherapy, or biological agents
* Received prior anti-cancer therapy for their pancreatic cancer
* Any condition or comorbidity that, in the opinion of the investigator, would interfere with evaluation of study treatment or interpretation of subject safety or study results, including but not limited to:
* Any major surgery or irradiation less than 4 weeks prior to baseline disease assessment
* Active infection (viral, fungal, or bacterial) requiring systemic therapy
* Known active hepatitis B virus, hepatitis C virus, or HIV infection
* Active tuberculosis as defined per local guidance
* History of allogeneic tissue/solid organ transplant
* Prior malignancy requiring active treatment within the previous 3 years except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast
* Pregnan…
What they're measuring
1
Incidence of adverse events
Timeframe: 30 days after treatment discontinuation