The Drug Rediscovery Protocol (DRUP Trial)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Netherlands Cancer Institute

About this trial

This is a prospective, non-randomized clinical trial that aims to describe the efficacy and toxicity of commercially available, targeted anticancer drugs\* prescribed for treatment of patients with advanced cancer with a potentially actionable variant as revealed by a genomic or protein expression test. The study also aims to simplify patient access to approved targeted therapies that are contributed to the program by collaborating pharmaceutical companies and to perform next generation sequencing on tumor biopsies for biomarker analyses. Eligible patients have an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma for which standard treatment options are no longer available and acceptable performance status and organ function. A genomic or protein expression test must have been performed on the tumor and the results must identify at least one potentially actionable molecular variant as defined in the protocol. Results from the molecular profiling test will be used to determine an appropriate drug(s) from among those available in the protocol. The choice of drug will be supported by a list of potential profiles, a molecular tumor board, a knowledge library and by study coordinators for review and approval of the match. The protocol-specified treatment will be administered to the patient once any drug-specific eligibility criteria are confirmed and a fresh pre-treatment biopsy is performed for future genetic studies. All patients who receive treatment with a drug available in the protocol will be followed for standard efficacy outcomes including tumor response, progression-free and overall survival as well as duration of treatment. In addition, treatment related toxicity will be evaluated.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult (age >18 years) patient with a histologically-proven locally advanced or metastatic solid tumor, multiple myeloma or B cell non-Hodgkin lymphomawith symptomatic disease progression or progression according to RECIST-criteria after standard anti-cancer treatment or for whom no such treatment is available or indicated.

ECOG performance status 0-2

Patients must have acceptable organ function as defined below. However, specific inclusion/

Disqualifiers

Absolute neutrophil count ≥ 1.5 x 109/l

Hemoglobin > 5.6 mmol/l

Platelets > 75 x 109/l

Total bilirubin < 2 x ULN

Trial design

Design model

Parallel

Treatments tested in this trial

  • Panitumumab

    Drug

    Panitumumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of panitumumab might be expected based on their molecular tumor profile.

  • Olaparib

    Drug

    Olaparib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of olaparib might be expected based on their molecular tumor profile.

  • Dabrafenib

    Drug

    Dabrafenib treatment for patients with an mutated advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of dabrafenib might be expected based on their molecular tumor profile.

  • Nilotinib

    Drug

    Nilotinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of nilotinib might be expected based on their molecular tumor profile.

  • Trametinib

    Drug

    Trametinib treatment for patients with an mutated advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of trametinib might be expected based on their molecular tumor profile.

  • Erlotinib

    Drug

    Erlotinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of erlotinib might be expected based on their molecular tumor profile.

  • Trastuzumab and Pertuzumab (combination treatment)

    Drug

    Trastuzumab and Pertuzumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of trastuzumab + pertuzumab might be expected based on their molecular tumor profile.

  • Vemurafenib and Cobimetinib (combination treatment)

    Drug

    Vemurafenib + Cobimetinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Vemurafenib + Cobimetinib might be expected based on their molecular tumor profile.

  • Vismodegib

    Drug

    Vismodegib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of vismodegib might be expected based on their molecular tumor profile.

  • Regorafenib

    Drug

    Regorafenib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of vismodegib might be expected based on their molecular tumor profile.

  • Nivolumab

    Drug

    Nivolumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of nivolumab might be expected based on their molecular tumor profile.

  • Afatinib

    Drug

    Afatinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Afatinib might be expected based on their molecular tumor profile.

  • Dabrafenib and trametinib

    Drug

    Dabrafenib + trametinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Dabrafenib + Trametinib might be expected based on their molecular tumor profile.

  • Ribociclib

    Drug

    Ribociclib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Ribociclib might be expected based on their molecular tumor profile.

  • Lenvatinib

    Drug

    Lenvatinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Lenvatinib might be expected based on their molecular tumor profile.

  • Pembrolizumab

    Drug

    Pembrolizumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Pembrolizumab might be expected based on their molecular tumor profile.

  • Durvalumab

    Drug

    Durvalumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Durvalumab might be expected based on their molecular tumor profile.

  • Rucaparib

    Drug

    Rucaparib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Rucaparib might be expected based on their molecular tumor profile.

  • Axitinib

    Drug

    Axitinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Axitinib might be expected based on their molecular tumor profile.

  • Palbociclib

    Drug

    Palbociclib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Palbociclib might be expected based on their molecular tumor profile.

  • Crizotinib

    Drug

    Crizotinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Crizotinib might be expected based on their molecular tumor profile.

  • Sunitinib

    Drug

    Sunitinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Sunitinib might be expected based on their molecular tumor profile.

  • Cabozantinib

    Drug

    Cabozantinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Cabozantinib might be expected based on their molecular tumor profile.

  • Abemaciclib

    Drug

    Abemaciclib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Abemaciclib might be expected based on their molecular tumor profile.

  • Alectinib

    Drug

    Alectinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Alectinib might be expected based on their molecular tumor profile.

  • Atezolizumab and Bevacizumab

    Drug

    Atezolizumab + Bevacizumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of Atezolizumab + Bevacizumab might be expected based on their molecular tumor profile.

  • Ipilimumab and nivolumab

    Drug

    Ipilimumab+nivolumab treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of ipilimimab + nivolumab might be expected based on their molecular tumor profile.

  • Entrectinib

    Drug

    Entrectinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of entrectinib might be expected based on their molecular tumor profile.

  • Talazoparib

    Drug

    Talazoparib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of talazoparib might be expected based on their molecular tumor profile.

  • Dacomitinib

    Drug

    Dacomitinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of dacomitinib might be expected based on their molecular tumor profile.

  • Lorlatinib

    Drug

    Lorlatinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of lorlatinib might be expected based on their molecular tumor profile.

  • Erdafitinib

    Drug

    Erdafitinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of erdafitinib might be expected based on their molecular tumor profile.

  • Alpelisib

    Drug

    Alpelisib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of alpelisib might be expected based on their molecular tumor profile.

  • Niraparib

    Drug

    Niraparib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of niraparib might be expected based on their molecular tumor profile.

  • Pemigatinib

    Drug

    Pemigatinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of pemigatinib might be expected based on their molecular tumor profile.

  • Selpercatinib

    Drug

    Selpercatinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of selpercatinib might be expected based on their molecular tumor profile.

  • Tepotinib

    Drug

    Tepotinib treatment for patients with an advanced solid tumor, multiple myeloma or B cell non-Hodgkin lymphoma, who are not eligible for on-label treatment but for whom anti-tumor activity of tepotinib might be expected based on their molecular tumor profile.

Treatment groups

1,550 Participants
are divided into 37 treatment groups

37

Treatment groups

See each treatment group below.

Group A: PanitumumabExperimental treatment 1 intervention
Group B: OlaparibExperimental treatment 1 intervention
Group C: DabrafenibExperimental treatment 1 intervention
Group D: NilotinibExperimental treatment 1 intervention
Group E: TrametinibExperimental treatment 1 intervention
Group F: ErlotinibExperimental treatment 1 intervention
Group G: Trastuzumab & Pertuzumab (combination)Experimental treatment 1 intervention
Group H: Vemurafenib & Cobimetinib (combination)Experimental treatment 1 intervention
Group I: VismodegibExperimental treatment 1 intervention
Group J: RegorafenibExperimental treatment 1 intervention
Group K: NivolumabExperimental treatment 1 intervention
Group L: AfatinibExperimental treatment 1 intervention
Group M: Dabrafenib & trametinib (combination)Experimental treatment 1 intervention
Group N: RibociclibExperimental treatment 1 intervention
Group O: LenvatinibExperimental treatment 1 intervention
Group P: PembrolizumabExperimental treatment 1 intervention
Group Q: DurvalumabExperimental treatment 1 intervention
Group R: RucaparibExperimental treatment 1 intervention
Group S: AxitinibExperimental treatment 1 intervention
Group T: PalbociclibExperimental treatment 1 intervention
Group U: CrizotinibExperimental treatment 1 intervention
Group V: SunitinibExperimental treatment 1 intervention
Group W: CabozantinibExperimental treatment 1 intervention
Group X: AbemaciclibExperimental treatment 1 intervention
Group Y: AlectinibExperimental treatment 1 intervention
Group Z: Atezolizumab/bevacizumabExperimental treatment 1 intervention
Group [: Ipilimumab/nivolumabExperimental treatment 1 intervention
Group \: EntrectinibExperimental treatment 1 intervention
Group ]: TalazoparibExperimental treatment 1 intervention
Group ^: dacomitinibExperimental treatment 1 intervention
Group _: LorlatinibExperimental treatment 1 intervention
Group `: ErdafitinibExperimental treatment 1 intervention
Group a: AlpelisibExperimental treatment 1 intervention
Group b: NiraparibExperimental treatment 1 intervention
Group c: PemigatinibExperimental treatment 1 intervention
Group d: SelpercatinibExperimental treatment 1 intervention
Group e: TepotinibExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of patients that are treated based on their molecular tumor profile

Primary outcome measure 1 is the percentage of submitted patients, that can be treated based on their molecular tumor profile within the context of this protocol.

Time frame
6 months after treatment initiation (estimated average)
2

Objective tumor response

Primary outcome measure 2 is the proportion of study participants with an objective tumor response upon study treatment..

Time frame
6 months after treatment initiation (estimated average)
3

Stable disease

Primary outcome measure 3 is the proportion of study participants that has stable disease (SD) during study treatment.

Time frame
6 months after treatment initiation (estimated average)
4

Treatment-related grade≥3 and serious adverse events

Primary outcome measure 4 is the proportion of patients that experience treatment-related grade≥3 and /or serious adverse events.

Time frame
6 months after treatment initiation (estimated average)

Secondary outcomes

1

Progression-free survival

Time frame
Up to 1 year after study completion
2

Overall survival

Time frame
Up to 1 year after study completion
3

Duration of treatment on study (time on drug)

Time frame
6 months after treatment initiation (estimated average)

Other outcomes

1

Concordance between pre-treatment and historic mutational tumor profile

Sequencing results of fresh pre-treatment biopsies will be available within 2 months after treatment initiation.

Time frame
2 months after treatment initiation (estimated average)

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The Netherlands Cancer Institute

Lead sponsor

Amgen

Collaborator

AstraZeneca

Collaborator

Bayer

Collaborator

Bristol-Myers Squibb

Collaborator

Novartis

Collaborator

Roche Pharma AG

Collaborator

Merck Sharp & Dohme LLC

Collaborator

Boehringer Ingelheim

Collaborator

Ipsen

Collaborator

Eisai Inc.

Collaborator

Pfizer

Collaborator

Clovis Oncology - Pharma and

Collaborator

Eli Lilly and Company

Collaborator

Janssen, LP

Collaborator

GlaxoSmithKline

Collaborator

Incyte Corporation

Collaborator

Dutch Cancer Society

Collaborator

Stelvio for Life

Collaborator