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NCT04897854RecruitingPhase 3

Timing of start of systemlc treatment for asymptomatic MEtastasized PANcreatic cancer (TIMEPAN): a prospective multicenter patient preference cohort

TIming of start of systemIc treatment for asymptomatic MEtastasized PANcreatic cancer (TIMEPAN): a prospective multicenter patient preference cohort

Source: EU CTIS (euclinicaltrials.eu) · Last updated 27 Oct 2026

Brief summary (registry, in English)

To assess the effect of immediate versus delayed start of chemotherapy on quality adjusted overall survival in patients with metastatic pancreatic cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
184 (estimated)
First submitted
2 Oct 2024
Start date
28 Oct 2024
Lead sponsor
Amsterdam UMC
NCT number
NCT04897854
EU CT number
2023-509465-20-00
EudraCT number
2019-004582-40

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 184
  • 12 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Other illness

  • New York Heart Association Class III or IV cardiac disease or myocardial infarction within the past 12 months

Lab values

  • Any other disease, active, uncontrolled bacterial, viral or fungal infection requiring systemic therapy, metabolic dysfunction, physical examination finding or clinical laboratory finding that leads to reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug, that may affect the interpretation of the results, or that may render the subject at high risk for treatment complications.

Other

  • Known central nervous system involvement or brain metastases.
  • Inability to comply with study and follow-up procedures as judged by the Investigator.
  • Women currently pregnant or breastfeeding.

Who the study is looking for

  • Signed, written Institutional Review Board/Ethics Committee-approved Informed Consent Form (ICF).
  • No prior chemotherapy for metastatic disease (patients might have received adjuvant treatment more than 3 months before the development of metastatic disease, or neoadjuvant treatment before surgery for resectable disease)
  • Patients with histologically/cytological confirmed diagnosis of metastatic pancreatic ductal adenocarcinoma or MDO consensus of metastatic disease. .
  • Measurable disease on computed tomography (CT) scan per RECIST version 1.1 criteria.
  • Eastern Cooperative Oncology Group Performance Status of 0-1
  • Life expectancy ≥ 3 months.
  • Age ≥ 18 years
  • A negative urine or serum pregnancy test within 7 days before Day 1 (first dose of study medication) if female subject is of childbearing potential.
  • Screening clinical laboratory values as follows: a. Absolute neutrophil count > 1.5 x 109 /L; b.Total bilirubin ≤ 1.5 times upper limit of normal (ULN).; c. Aspartate aminotransferase and alanine aminotransferase ≤ 2.5 times ULN, (if liver metastases are present, then ≤ 5 times ULN is allowed); d.Serum creatinine < 1.5 x ULN or creatinine clearance >50 mL/min/1.73 m2; e. Platelet count > 100,000 x 109 /L
  • No symptoms related to advanced disease, specified as: a. no pain requiring regular narcotic analgesics; b. no weight loss over 5 kg (unless related to surgery or other illness); c. no persistent nausea requiring medication; d. no obstructive bowel symptoms; e. no persistent fever related to metastatic cancer; f. no other symptom which in the opinion of the clinician was due to progressive metastatic cancer.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Meander Medisch Centrum
Coordinator of this site? Confirm its status
AmersfoortNetherlandsRecruiting
Amsterdam UMC Stichting
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AmsterdamNetherlandsRecruiting
Medisch Spectrum Twente
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EnschedeNetherlandsRecruiting
Ziekenhuis St Jansdal
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HarderwijkNetherlandsRecruiting
Spaarne Gasthuis Stichting
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HoofddorpNetherlandsRecruiting
Dijklander Ziekenhuis
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Hoorn NhNetherlandsRecruiting
Leids Universitair Medisch Centrum (LUMC)
Coordinator of this site? Confirm its status
LeidenNetherlandsRecruiting
Academisch Ziekenhuis Maastricht
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MaastrichtNetherlandsRecruiting
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
Coordinator of this site? Confirm its status
RotterdamNetherlandsRecruiting
Jeroen Bosch Ziekenhuis Stichting
Coordinator of this site? Confirm its status
'S-HertogenboschNetherlandsRecruiting
Diakonessenhuis Stichting
Coordinator of this site? Confirm its status
UtrechtNetherlandsRecruiting
St Antonius Ziekenhuis
Coordinator of this site? Confirm its status
UtrechtNetherlandsRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.