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NCT04704219 · FLOW

Participant flow

Pembrolizumab Plus Lenvatinib for First-line Advanced/Metastatic Non-clear Cell Renal Cell Carcinoma (1L nccRCC) (MK-3475-B61) · Source last updated 2025-12-03

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups
  1. description
    Participants with non-clear cell Renal Cell Carcinoma (nccRCC) received 400 mg Pembrolizumab (Pembro) intravenously (IV) on Day 1 of a 42-day cycle (every 6 weeks (Q6W)) for approximately 2 years PLUS 20 mg Lenvatinib (Lenva) orally once daily (QD) on Days 1 and 22 of a 42-day cycle (Q6W). Participants continued study intervention until progressive disease or discontinuation.
    id
    FG000
    title
    Pembrolizumab + Lenvatinib
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Screen Failure
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        78
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        80
      type
      Participants Ongoing
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        160
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        158
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        6
      type
      Second Course Treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        160
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Per protocol, six participants who experienced progression of Renal Cell Carcinoma (RCC) by radiographic evaluation continued second course treatment.
recruitment Details
This study was conducted at 56 centers in 14 countries.
Complete source fields
groups
  1. description
    Participants with non-clear cell Renal Cell Carcinoma (nccRCC) received 400 mg Pembrolizumab (Pembro) intravenously (IV) on Day 1 of a 42-day cycle (every 6 weeks (Q6W)) for approximately 2 years PLUS 20 mg Lenvatinib (Lenva) orally once daily (QD) on Days 1 and 22 of a 42-day cycle (Q6W). Participants continued study intervention until progressive disease or discontinuation.
    id
    FG000
    title
    Pembrolizumab + Lenvatinib
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Screen Failure
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        78
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        80
      type
      Participants Ongoing
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        160
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        158
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        6
      type
      Second Course Treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        160
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Per protocol, six participants who experienced progression of Renal Cell Carcinoma (RCC) by radiographic evaluation continued second course treatment.
recruitment Details
This study was conducted at 56 centers in 14 countries.

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Preserved source evidence · Not medical advice