A Dose Finding and Expansion Study of RO7051790 Administered Orally in Participants With Relapsed, Extensive-Stage Disease Small Cell Lung Cancer (ED SCLC)

  • Cancer
  • Lung Cancer
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:


This trial runs in
  • Barcelona
  • Birmingham
  • København
  • Madrid
  • Ottawa
  • Toronto
  • Villejuif
Trial Identifier:

NCT02913443 2016-001942-25 NP39148

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

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      Trial Summary

      This is a Phase I, open-label, multicenter study designed to assess the safety and tolerability of RO7051790 in participants with relapsed ED SCLC. This dose escalation and expansion study plans to determine the maximum tolerated dose and/or optimal biological dose as a recommended Phase 2 dose for RO7051790, based on the safety, tolerability, pharmacokinetic and pharmacodynamic profiles observed after oral administration of RO7051790.

      Hoffmann-La Roche Sponsor
      Phase 1 Phase
      NCT02913443,NP39148,2016-001942-25 Trial Identifier
      RO7051790 Treatments
      Small Cell Lung Cancer Condition
      Official Title

      A Multi-Center, Open Label, Phase I, Dose Finding and Expansion Study of RO7051790 Administered Orally in Patients With Relapsed, Extensive-Stage Disease Small Cell Lung Cancer (ED SCLC)

      Eligibility Criteria

      All Gender
      ≥ 18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Life expectancy greater than or equal to (>=) 12 weeks
      • Participants must have histologically or cytologically confirmed diagnosis of SCLC
      • Participants must have recurrent or refractory disease after receiving at least one prior platinum-containing chemotherapy regimen, or standard therapy is refused or not suitable. For participants in Canada: participants should also not be suitable for treatment with topotecan hydrochloride
      • Acute toxicities from any prior treatment, surgery, or radiotherapy must be National Cancer Institute-Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.03 Grade less than or equal to (<=) 1
      • Measureable disease per RECIST v1.1 prior to administration of study medication
      • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
      • Adequate bone marrow function
      • Adequate renal function
      • Participant must be able to swallow and retain orally administered study treatment
      • Women of childbearing potential and men should agree to use an effective form of contraception and to continue its use for the duration of study treatment and for a period of time after the last dose of study treatment
      Exclusion Criteria
      • Active malignancy other than SCLC within the previous 5 years
      • Participants who have received radiotherapy less than 2 weeks prior to first dose of study medication
      • Surgical procedure or clinically significant trauma within 2 weeks of first dose of study treatment
      • Treatment with any investigational agent <=3 weeks prior to first dose of study treatment
      • Participants with gastrectomy or pre-existing gastrointestinal disorders that may interfere with the proper absorption of the drug(s), as per conclusion of the clinical Investigator
      • Participants medicated with anti-depressants reported to have lysine-specific histone demethylase 1A (KDM1A)/lysine (K)-specific demethylase 1A (LSD1) inhibitory activity (such as tranylcypromine or phenelzine) within 28 days of treatment start
      • History of allergic reactions attributed to components of the formulated product(s)
      • History of seizure disorders
      • Participants with untreated central nervous system metastases, or history of previously treated disease. Participants must have stable hematological parameters, satisfying eligibility, platelet count must be stable for >=2 weeks prior to study drug administration
      • Participants who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study
      • Participants with evidence of electrolyte imbalance
      • Participants who are pregnant or breastfeeding
      • Participants who refuse to potentially receive blood products and/or have a hypersensitivity to blood products
      • Participants with known bone marrow disorders which may interfere with bone marrow recovery or participants with delayed recovery from prior chemoradiotherapy
      • Participants with known coagulopathy, platelet disorder or history of non-drug-induced thrombocytopenia
      • Hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV)-positive participants with active infection
      • Use of strong Cytochrome P450 3A4 (CYP3A4) inducers while on study medication
      • Participants with abnormal hepatic function
      • Participants with history of clinically significant bleeding, specifically any history of intracranial hemorrhage/hemorrhagic cardiovascular accident (CVA), or participants with gastrointestinal bleeding within the 12 months prior to study entry
      • Participants receiving therapeutic anti-coagulation or anti-platelet (anti-aggregant) therapies, except for therapeutic enoxaparin or low dose aspirin. Use of subcutaneous heparin prophylaxis, including low molecular weight heparin is also permitted

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