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NCT04056247Active, not recruiting

Predicting Responsiveness in Oncology Patients Based on Host Response Evaluation During Anti Cancer Treatments

PROPHETIC - Predicting Responsiveness in Oncology Patients Based on Host Response Evaluation During Anti Cancer Treatments

Source: ClinicalTrials.gov · Last updated 19 Oct 2026

Brief summary (registry, in English)

The PROPHETIC study is a prospective, multi-center, international clinical study aimed at developing an algorithm to predict patient outcomes. The study involves analyzing the proteomic profiles of patients undergoing therapy to assess the likelihood of clinical benefit from their prescribed treatment. Blood samples are collected prior to and during the treatment period and analyzed as part of the ongoing development of thealgorithm.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
11 Aug 2019
Start date
1 Oct 2019
Primary completion date
1 Oct 2029
Lead sponsor
OncoHost Ltd.
NCT number
NCT04056247

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 1 Oct 2019 to the primary completion date, 1 Oct 2029
  • 41 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent and/or other active malignancy that has required systemic treatment within 2 years of first dose of study drug

Other illness

  • Generalized impairment or mental incompetence that would render the patient unable to understand his/her participation in the study.

Who the study is looking for

  • Provision of informed consent prior to any study-specific procedures.
  • Male or female aged at least 18 years.
  • ECOG PS - 0/1-2
  • Normal hematologic, renal and liver function:
    • Absolute neutrophil count higher than 1500/mm3
    • Platelets count higher than 100,000/mm3
    • haemoglobin higher than 9 g/dL
    • Creatinine concentration ≤1.4 mg/dL, or creatinine clearance higher than 40 mL/min
    • Total bilirubin lower than 1.5 mg/dL, ALT and AST levels ≤ 3 times above the upper normal limit.
  • At least one measurable lesion in order to enable the assessment of the response (except for stage IIIb-d malignant melanoma patients).

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

Full criteria on ClinicalTrials.gov

Sites (41)

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

SiteCityCountrySite status
Asklepois
Coordinator of this site? Confirm its status
GautingGermanyUnknown status
Thoraxklinik Heidelberg gGmbH
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HeidelbergGermanyUnknown status
044 Hospital Universitario Virgen Macarena
Coordinator of this site? Confirm its status
SevilleSpainUnknown status
Aberdeen Royal Infirmary
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AberdeenUnited KingdomUnknown status
Royal Bournemouth General Hospital
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BournemouthUnited KingdomUnknown status
Bradford Teaching Hospitals
Coordinator of this site? Confirm its status
BradfordUnited KingdomUnknown status
Cheltenham General Hospital
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CheltenhamUnited KingdomUnknown status
Withybush Hospital
Coordinator of this site? Confirm its status
HaverfordwestUnited KingdomUnknown status
Mount Vernon Cancer Centre
Coordinator of this site? Confirm its status
NorthwoodUnited KingdomUnknown status
The Shrewsbury and Telford Hospital
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ShrewsburyUnited KingdomUnknown status
South Tyneside
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South ShieldsUnited KingdomUnknown status
Lister Hospital
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StevenageUnited KingdomUnknown status
Sunderland Royal Hospital
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SunderlandUnited KingdomUnknown status
Swansea Bay UHB Singleton Hospital
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SwanseaUnited KingdomUnknown status
Torbay Hospital
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TorquayUnited KingdomUnknown status
Haemek Medical Center
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AfulaIsraelUnknown status
Barzilai Medical Center
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AshkelonIsraelUnknown status
Soroka Medical Center
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BeershebaIsraelUnknown status
Shamir Medical Center
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Be’er Ya‘aqovIsraelUnknown status
Bnai Zion Medical Center
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HaifaIsraelUnknown status
Rambam Medical Center
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HaifaIsraelUnknown status
Hadassah Medcial Center
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JerusalemIsraelUnknown status
Meir Medical Center
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Kfar SabaIsraelUnknown status
Rabin Medical Center
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Petah TikvaIsraelUnknown status
Kaplan Medical Center
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RehovotIsraelUnknown status
Sourasky Medical Center
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Tel AvivIsraelUnknown status
Assuta Medical Cetner
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Tel AvivIsraelUnknown status
Sheba Medical Center
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Tel AvivIsraelUnknown status
Sheba medical center
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Tel HaShomerIsraelUnknown status
Birmingham VAHCS
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BirminghamUnited StatesUnknown status
Roswell Park
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BuffaloUnited StatesUnknown status
Helen Nassif Community Cancer Center
Coordinator of this site? Confirm its status
Cedar RapidsUnited StatesUnknown status
West Clinic
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GermantownUnited StatesUnknown status
Michael E. DeBakey VA Medical Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Mayo Clinic
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JacksonvilleUnited StatesUnknown status
University of Miami
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MiamiUnited StatesUnknown status
Rutgers Cancer Institute
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New BrunswickUnited StatesUnknown status
Florida Cancer Specialist and Research Institute
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OrlandoUnited StatesUnknown status
Protean Biodiagnosics
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OrlandoUnited StatesUnknown status
Northwest Community Healthcare
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Rolling MeadowsUnited StatesUnknown status
151-Christus Health St. Michael
Coordinator of this site? Confirm its status
TexarkanaUnited StatesUnknown status

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