N
← Back to Search
Sponsored

Accelerate Your Clinical Trial Recruitment

Reach thousands of high-intent patients matching your specific inclusion criteria.

Start Campaign
RECRUITING Phase 3 ClinicalTrials.gov

A Rollover Study for Participants Previously Enrolled in a Genentech and/or F. Hoffman-La Roche Sponsored Study

Sponsor: Hoffmann-La Roche • ClinicalTrials.gov ID: NCT05862285

Registry updated: 2026-10-02
Ad

Recruiting for Similar Conditions?

Sponsors are looking for patients like you. See if you qualify for compensated research studies.

Check Eligibility →

Description

The purpose of this extension study is to provide continued treatment with Roche investigational medicinal product (IMP\[s\]) monotherapy or Roche IMP(s) combined with other agent(s) or comparator agent(s) for eligible participants with cancer who are still on study treatment at the time of roll-over from the parent study and who do not have access to the study treatment locally.

Interventions

  • Ipatasertib (Drug)
    Ipatasertib will be administered as a monotherapy at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Tiragolumab (Drug)
    Tiragolumab in combination with atezolizumab will be administered at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Atezolizumab (Drug)
    Atezolizumab will be administered as a monotherapy and in combination at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants' discontinuation from the parent study.
  • Tiragolumab and Atezolizumab (Drug)
    Tiragolumab and Atezolizumab in fixed dose combination administered intravenously (IV) at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Bevacizumab (Drug)
    Bevacizumab will be administered as a monotherapy or in combination with atezolizumab at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Entrectinib (Drug)
    Entrectinib will be administered as a monotherapy at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Inavolisib (Drug)
    Inavolisib will be administered as a monotherapy or in combination at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.
  • Divarasib (Drug)
    Divarasib will be administered as a monotherapy or in combination with atezolizumab or bevacizumab at the same dose, schedule, and with the same administration guidelines that were in effect at the time of participants discontinuation from the parent study.

Eligibility criteria

Inclusion Criteria: * Eligible for continuing Roche IMP-based therapy at the time of roll-over from the parent study, as per the parent study protocol OR * Eligible for continuing the comparator agent(s) in a Genentech- or Roche-sponsored study as per the parent study protocol, with no access to commercially available comparator agent * First dose of study treatment in this extension study will be received within 7 days of the treatment interruption window allowed by the parent study * Continue to benefit from the Roche IMP-based therapy or comparator at the time of roll-over from the parent study as assessed by the investigator * Ability to comply with the extension study protocol, per Investigator's judgement Exclusion Criteria: * Meet any of the study treatment discontinuation criteria specified in the parent study at the time of enrollment in this extension study * Study treatment or comparator agent is commercially marketed in the participant's country for the participant-specific disease and is accessible to the participant * Treatment with any anti-cancer treatment (other than treatment permitted in the parent study) during the time between last treatment in the parent study and the first dose of study treatment in this extension study * Permanent discontinuation of all study treatment(s) or comparator agent(s) for any reason during the parent study or during the time between last treatment in the parent study and the first dose of study treatment in this extension study (if applicable) * Ongoing SAE(s) that has not resolved to baseline level or Grade ≤1 from the parent study or during the time between the last treatment in the parent study and the first dose of study treatment in this extension study * Concurrent participation in any therapeutic clinical trial (other than the parent study)

Conditions

Cancer

Locations

  • GHdC Site Les Viviers — Charleroi, Belgium
  • AZ Groeninge — Kortrijk, Belgium
  • UZ Leuven Gasthuisberg — Leuven, Belgium
  • Princess Margaret Cancer Center — Toronto, Ontario, Canada
  • Xiehe Hospital, Tongji Medical College Huazhong University of Science & Technology — Wuhan, Hubei, China
  • First Affiliated Hospital of Medical College of Xi'an Jiaotong University — XI 'an City, Shaanxi Province, Shaanxi, China
  • Fudan University Shanghai Cancer Center — Shanghai, Shanghai Municipality, China
  • Beijing Cancer Hospital — Beijing, China
  • the First Hospital of Jilin University — Changchun, China
  • West China Hospital of Sichuan University — Chengdu, China
  • Cancer Center of Guangzhou Medical University — Guangzhou, China
  • Nanfang Hospital, Southern Medical University — Guangzhou, China
  • Zhejiang People's Hospital — Hangzhou, China
  • Sir Run Run Shaw Hospital Zhejiang University — Hangzhou, China
  • Zhejiang Cancer Hospital — Hangzhou, China
  • Harbin Medical University Cancer Hospital — Harbin, China
  • The Second Affiliated Hospital of Anhui Medical University — Hefei, China
  • Meizhou People's Hospital — Meizhou, China
  • The 1st Affiliated Hospital of Nanchang Unversity — Nanchang, China
  • Jiangsu Province Hospital of Chinese Medicine — Nanjing, China
  • Fudan University Shanghai Cancer Center — Shanghai, China
  • Shanghai Geriatric Medical Center — Shanghai, China
  • Tianjin Cancer Hospital — Tianjin, China
  • First Affiliated Hospital of Medical College of Xi'an Jiaotong University — Xi'an, China
  • The First Affiliated Hospital of Xiamen University — Xiamen, China
  • The First Affiliated Hospital of Xinxiang Medical University — Xinxiang, China
  • Henan Cancer Hospital — Zhengzhou, China
  • Clinica CIMCA — San José, Costa Rica
  • ICIMED Instituto de Investigación en Ciencias Médicas — San José, Costa Rica
  • AP-HM- Hôpital de La Timone — Marseille, Bouches-du-Rhône, France
  • Institut Bergonie — Bordeaux, France
  • Centre Francois Baclesse — Caen, France
  • Institut de Cancérologie de Bourgogne — Dijon, France
  • Centre Leon Berard — Lyon, France
  • Hopital de la Timone — Marseille, France
  • Centre Régional de Lutte Contre Le Cancer Val D'aurelle Paul Lamarque — Montpellier, France
  • CHU de Nantes - Hotel Dieu — Nantes, France
  • Institut de cancerologie du Gard — Nîmes, France
  • Institut Curie — Paris, France
  • Hopital Tenon — Paris, France
  • ICO - Site René Gauducheau — Saint-Herblain, France
  • Institut Claudius Regaud — Toulouse, France
  • Gustave Roussy — Villejuif, France
  • General Hospital "G.Papanikolaou" — Asvestochóri, Greece
  • Metropolitan General Hospital — Cholargós, Greece
  • National Cancer Center Hospital East — Chiba, Japan
  • Kyushu University Hospital — Fukuoka, Japan
  • Toranomon Branch Hospital — Kanagawa, Japan
  • Yokohama City University Medical Center — Kanagawa, Japan
  • Kanagawa Cancer Center — Kanagawa, Japan
  • National Cancer Center Hospital East — Kashiwa-shi, Japan
  • Saitama Cancer Center — Saitama, Japan
  • NHO Kinki-Chuo Chest Medical Center — Sakaishi, Japan
  • Centro Medico Culiacan SA de CV — Culiacán, Sinaloa, Mexico
  • Medical Care & Research — Mérida, Yucatán, Mexico
  • Consultorio de Especialidad en Urologia Privado — Durango, Mexico
  • Uniwersyteckie Centrum Kliniczne — Gda?sk, Poland
  • Szpital Wojewódzki im. Miko?aja Kopernika — Koszalin, Poland
  • Narodowy Instytut Onkologii im. M.Sklodowskiej-Curie — Warsaw, Poland
  • Russian Scientific Center of Roentgenoradiology — Moscow, Moscow Oblast, Russia
  • Moscow City Oncology Hospital #62 — Moscow, Moscow Oblast, Russia
  • P.A. Herzen Oncological Inst. — Moscow, Moscow Oblast, Russia
  • National Cancer Center — Goyang-si, South Korea
  • CHA Bundang Medical Center — Gyeonggi-do, South Korea
  • Seoul National University Bundang Hospital — Seongnam-si, South Korea
  • Asan Medical Center — Seoul, South Korea
  • Samsung Medical Center — Seoul, South Korea
  • Taichung Veterans General Hospital — Taichung, Taiwan
  • National Cheng Kung University Hospital — Tainan, Taiwan
  • National Taiwan University Hospital — Taipei, Taiwan
  • Chang Gung Memorial Hospital - Linkou — Taoyuan, Taiwan
  • Chulalongkorn Hospital — Bangkok, Thailand
  • Siriraj Hospital — Bangkok, Thailand
  • Maharaj Nakorn Chiangmai Hospital — Chiang Mai, Thailand
  • Arensia Exploratory Medicine - Ukraine — Kyiv, Ukraine
  • Leicester Royal Infirmary — Leicester, United Kingdom
  • Royal Marsden Hospital - Surrey — Surrey, United Kingdom
Sponsored

Partner with Nurenyx

Showcase your study to thousands of motivated patients matching your criteria.

Learn More

Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record