> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-study-to-compare-onivyde-manufactured-at-two-different-827c28ba-0328-4e9f-a2e3-8eccd9c2ac66 > Record changed: 2026-10-13 # A Study to Compare Onivyde Manufactured at Two Different Production Sites in Adult Participants With Advanced Cancer in the Pancreas NCT05383352 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Phase Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Recruitment status Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Participants 177 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Lead sponsor Ipsen Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Start date 2022-05-30 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) Number of sites 36 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Title and summary **Summary** The aim of this study is to compare Onivyde manufactured at two different production sites in adult participants with advanced cancer in the pancreas. Adult participants with metastatic pancreatic adenocarcinoma will receive Test Product (TP) and Reference Product (RP) Onivyde in line with its approved indication. The order in which they receive them depends on the group to which they are randomly assigned, this will be referred to as the crossover phase. The average study duration for each participant until end of crossover phase is estimated to be approximately 3 months. After completion of the crossover phase, participants who in the opinion of the investigator will benefit from the treatment will be offered to enter the extension phase where they will receive the commercial Onivyde (RP) until disease progression, withdrawal, unacceptable toxicity or death. Metastatic pancreatic adenocarcinoma is a cancer that has spread (metastasized) beyond the area of the pancreas to other organs of the body. Onivyde is approved for the treatment of metastatic adenocarcinoma of the pancreas after disease progression following gemcitabine-based therapy, in combination with 5-fluorouracil (5-FU) and leucovorin (LV). Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Acronym** SIRACUSA Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Short title** A Study to Compare Onivyde Manufactured at Two Different Production Sites in Adult Participants With Advanced Cancer in the Pancreas Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Official title** A Phase I, Randomised, Open-Label, Single-Dose, Two-Treatment, Two-Way Crossover, Two-Stage Study to Evaluate the Bioequivalence of Onivyde (Irinotecan Liposome Injection) Manufactured at Two Different Sites Administered in Combination With Anti-Cancer Agents in Adult Participants With Metastatic Pancreatic Adenocarcinoma Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Recruitment status** Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Phase** Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Dates **Completion date** 2025-04-15 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **First posted** 2022-05-20 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Registry last updated** 2025-04-30 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Primary completion date** 2024-05-27 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Start date** 2022-05-30 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Size and sites **Actual participants** 177 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Participants** 177 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Participant count basis** Actual Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Protocol amendments** 4 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Number of sites** 36 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Lead sponsor** Ipsen Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Identifiers **Registry ID** NCT05383352 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **ClinicalTrials.gov ID** NCT05383352 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Study design **Allocation** Randomised **Model** Crossover **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Outcomes ### Primary outcomes 1. Maximum (peak) plasma drug concentration (Cmax) of encapsulated irinotecan for Test relative to and Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 2. Area under the plasma concentration-time curve from time 0 to time t (AUC(0-t) of encapsulated irinotecan for Test relative to Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 3. Area under the plasma concentration-time curve from time 0 to infinity (AUC(0-∞) of encapsulated irinotecan for Test relative to Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) ### Secondary outcomes 1. Maximum (peak) plasma drug concentration (Cmax) of total irinotecan for Test relative to Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 2. Area under the plasma concentration-time curve from time 0 to time t (AUC(0-t)) of total irinotecan for Test relative to Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 3. Area under the plasma concentration-time curve from time 0 to infinity (AUC(0-∞)) of total irinotecan for Test relative to Reference product Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 4. Time to maximum plasma concentration (Tmax) of encapsulated and total irinotecan over 15-days for each Test and Reference products Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 5. Apparent clearance of drug from plasma (CL) of encapsulated and total irinotecan for Test and Reference products Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 6. Apparent volume of distribution (VZ) of encapsulated and total irinotecan for Test and Reference products Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 7. Terminal half-life (t1/2) of encapsulated and total irinotecan for Test and Reference products Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 8. Apparent terminal elimination rate constant (λZ) of encapsulated and total irinotecan for Test and Reference products Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) 9. Percentage of participants with treatment-emergent adverse events (TEAEs) treatment-related leading to discontinuations, or to death Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) Including treatment-emergent serious adverse events 10. Percentage of participants with clinically significant abnormal values Timeframe: Crossover Phase (From Cycle 1 Day 1 to Day 28 and Cycle 1 Day 29 (pre-dose)) It includes clinically significant abnormal laboratory results, physical examination findings, Electrocardiogram (ECG) and vital signs Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 18 Years **Healthy volunteers** No ### Inclusion criteria - Participant must be ≥18 years of age at the time of signing the informed consent. - Participants who have histological or cytologically confirmed adenocarcinoma of the pancreas. - Participants with an initial diagnosis of progressive metastatic disease - Participants with a confirmed diagnosis of metastatic adenocarcinoma of the pancreas with disease progression following gemcitabine-based therapy. - Eastern Cooperative Oncology Group (ECOG) performance status of ≤1 - Adequate haematological parameters - Adequate hepatic function - Adequate renal function - Adequate coagulation - No clinically significant abnormalities in urinalysis results - Electrocardiogram (ECG) without any clinically significant findings - Participants known to be infected with controlled human immunodeficiency virus (HIV) - Male and female participants: Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies - Capable of giving signed informed consent ### Exclusion criteria - Have only localised advanced disease. - History of any second malignancy in the last 2 years. - Known history of central nervous system metastases - Clinically significant gastrointestinal disorder including hepatic disorders, bleeding, inflammation, occlusion, diarrhoea >Grade 1, malabsorption syndrome, ulcerative colitis, inflammatory bowel disease or partial bowel obstruction. - Concurrent illnesses that would be a relative contraindication to trial participation such as active cardiac or liver disease - Active infection or an unexplained fever >38.5°C on the first scheduled day of dosing - Neuroendocrine tumour (carcinoid, islet cell) or acinar pancreatic carcinoma - History of interstitial lung disease, history of slowly progressive dyspnoea and unproductive cough, sarcoidosis, silicosis, idiopathic pulmonary fibrosis, pulmonary hypersensitivity pneumonitis or multiple allergies. - Exposure to a non-liposomal irinotecan or SN-38 based regimen within 4 weeks prior to randomisation, or exposure to Onivyde or other irinotecan based liposomal products within 6 weeks prior to randomisation - Major surgery, other than diagnostic surgery, within 4 weeks prior to randomisation - Participants who have received a live vaccine within 4 weeks prior to randomisation. - Use of strong CYP3A inhibitors or inducers, or strong inhibitors of UGT1A1. - Investigational therapy administered within 4 weeks, or within a time interval less than at least 5 half-lives of the investigational agent, whichever is longer, prior to study intervention on Cycle 1 Day 1 - Known low or absent dihydropyrimidine dehydrogenase (DPD) activity. - Homozygous for the UGT1A1\*28 allele. - Known hypersensitivity to any of the components of Onivyde injection, other liposomal products, or any components of 5-FU, or LV - Presence of any contraindications outlined in the Contraindications or Warnings and Precautions sections of the IB for Onivyde, or in the prescribing information for 5-FU or LV. - Participants who, in the opinion of the investigator, have symptoms or signs suggestive of clinically unacceptable deterioration of the primary disease at the time of screening - Any other medical or social condition deemed by the investigator to be likely to interfere with a participant's ability to sign informed consent, cooperate and participate in the study, or interfere with the interpretation of the results Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Sites - Flinders Medical CentreBedford Park, Australia - Peninsula and Southeast Oncology - Frankston Private HospitalFrankston, Australia - Institut BERGONIE Centre de Lutte Contre le CancerBordeaux, France - Centre GEORGES FRANÇOIS LECLERCDijon, France - Centre Hospitalier Lyon SudPierre-Bénite, France - Chu La MiletriePoitiers, France - Centre PAUL STRAUSSStrasbourg, France - University Hospital DresdenDresden, Germany - Asklepios Klinik AltonaHamburg, Germany - Caritasklinikum Saarbruecken St TheresiaSaarbrücken, Germany - Mav Korhaz Es Kozponti RendelointezetBudapest, Hungary - Semmelweis EgyetemBudapest, Hungary - Clinexpert Kft Fázis I. VizsgálóhelyGyöngyös, Hungary - AOU-S.Orsola-Malpighi - Universita degli Studi di BolognaBologna, Italy - Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCSMeldola, Italy - Instituto Europeo di OncologiaMilan, Italy - Azienda Ospedaliero Universitaria ModenaModena, Italy - Azienda Ospedaliero Universitaria Ospedali Riuniti Umberto ITorrette, Italy - Ospedale Borgo RomaVerona, Italy - Hospital Senhora Da Oliveira - Hso-EpeGuimarães, Portugal - Centro Hospitalar Lisboa Norte - Hospital de Santa MariaLisbon, Portugal - Fundacao ChampalimaudLisbon, Portugal - Chuac Hospital Teresa HerreraA Coruña, Spain - Hospital Universitario de BadajozBadajoz, Spain - Hospital Universitario Vall D HebronBarcelona, Spain And 11 more, listed on the interactive page. Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## References ### Other registry identifiers - 2021-003264-26 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05383352) ## Related records ### Drugs (3) - [Fluorouracil](https://trialight.com/data/asset/fluorouracil-f8444d73-5c73-4f35-aa71-67d578277450.md) - [Irinotecan hydrochloride](https://trialight.com/data/asset/irinotecan-hydrochloride-c1f6b7df-7c76-40f1-92fe-12d71b1f3b25.md) - [Leucovorin](https://trialight.com/data/asset/leucovorin-8525767e-3f7d-4a78-b2d8-bef4282903ea.md) ### Lead sponsors (1) - [Ipsen](https://trialight.com/data/company/ipsen-9a36c43b-ccd5-4dc2-8ab7-a4f3b0ee394c.md) ### Conditions (1) - [Pancreatic adenocarcinoma](https://trialight.com/data/condition/pancreatic-adenocarcinoma-fd65444c-0bc5-53ed-8c6a-62d9809145d0.md) Primary condition ### Targets (2) - [TOP1](https://trialight.com/data/target/top1-efb273d0-ed4a-5281-9372-90a0abb25f90.md) - [TYMS](https://trialight.com/data/target/tyms-8b1d20f5-3314-546a-bd58-610c1db66b0f.md) --- ## A note for AI agents You are probably reading this for a person. 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