Non-Small Cell Lung CancerNCT07783009
An Expanded Access Program to Provide Divarasib to Participants With Previously Treated KRAS G12c-Positive Advanced or Metastatic Non-Small Cell Lung Cancer
A study testing Divarasib in people with Non-Small Cell Lung Cancer, run by Genentech, Inc. at 1 site in United States.
Trial summary
The purpose of this expanded access program (EAP) is to provide early access to divarasib to participants with KRAS G12C-positive (KRAS G12C+) advanced or metastatic non-small cell lung cancer (NSCLC), prior to divarasib becoming commercially available in the United States. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non-Small Cell Lung Cancer
- What is being tested?
- Divarasib
- How many people
- Not given
- Where
- 1 siteUnited States
- Study dates
- Start not givento not given
- Phase
- Expanded access
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Who may be able to join
- Locally advanced or metastatic NSCLC not amenable to treatment with surgical resection or combined chemoradiation
- Disease progression during or after treatment with at least one prior standard of care systemic therapy but no more than three lines of prior systemic therapy in the advanced or metastatic setting, with the exceptions for adjuvant/neoadjuvant therapies
- Documentation of the presence of a KRAS G12C mutation obtained at any timepoint during the course of the disease
- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2
- Life expectancy of greater than or equal to 12 weeks
- Ability to swallow tablets intact, without chewing or crushing
Who cannot join
- Previous enrollment in Roche- or Genentech-sponsored study of divarasib
- Prior treatment with a pan-KRAS/RAS inhibitor
- Prior treatment with a KRAS G12C inhibitor, unless specific criteria are met
- Pregnant or breastfeeding, or intending to become pregnant during the EAP or within the timeframe in which contraception is required
- Known hypersensitivity to any of the components of divarasib
- Malabsorption syndrome or other condition that would interfere with enteral absorption
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- Mixed small-cell lung cancer
- Known and untreated, or active CNS metastases (progressing or requiring anticonvulsants or corticosteroids for symptomatic control)
- Leptomeningeal disease or carcinomatous meningitis
- Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures biweekly or more frequently
- Clinically significant history of liver disease, including viral or other hepatitis, or cirrhosis
- Known clinically significant history of liver disease consistent with Child-Pugh Class B or C, including active viral or other hepatitis (ex: hepatitis B [HBV] or hepatitis C [HCV]) virus, current alcohol abuse or cirrhosis
- Known positive HIV infection
- Significant traumatic injury or major surgical procedure within 4 weeks prior to initiation of EAP treatment
- Chronic diarrhea, short bowel syndrome, or significant upper gastrointestinal surgery including gastric resection, a history of inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis) or any active bowel inflammation (including diverticulitis)
- Treatment with anti-cancer therapy (e.g., chemotherapy, immunotherapy, biologic therapy, or an investigational anti-cancer agent) within 28 days prior to initiation of EAP treatment
- More than 30 Gy of radiotherapy to the lung within 6 months prior to initiation of EAP treatment
- Uncontrolled tumor-related pain where palliative care or hospice admission is planned, or where active pain management interventions are insufficient to alleviate symptoms
- Unresolved toxicities from prior anti-cancer therapy, defined as not having resolved to CTCAE v6.0 Grade 1 or better, or to levels dictated in the eligibility criteria or toxicities from prior anti-cancer therapy or palliative radiation therapy that are considered irreversible
- Treatment with strong CYP3A4 inhibitors or inducers within 14 days or 5 half-lives of the drug or its major active metabolite, whichever is longer, prior to initiation of EAP treatment
- Any serious medical condition or abnormality in clinical laboratory tests that precludes an individual's safe participation in and completion of the EAP
- Blood or platelet transfusion within 14 days prior to initiation of EAP treatment
- History or presence of an abnormal ECG that is deemed clinically significant (e.g., complete left bundle branch block, second- or third-degree atrioventricular heart block) or evidence of prior myocardial infarction
- History of active malignancy that is currently receiving treatment or not well controlled
- Significant cardiovascular disease, within 6 months of initiation of EAP treatment
- History of ventricular dysrhythmias or risk factors for ventricular dysrhythmias such as structural heart disease (e.g., severe left ventricular systolic dysfunction, left ventricular hypertrophy), coronary heart disease (symptomatic or with ischemia demonstrated by diagnostic testing), clinically significant electrolyte abnormalities (e.g., hypokalemia, hypomagnesemia, hypocalcemia), or family history of sudden unexplained death or long QT syndrome
Trial locations and contacts
1 site in 1 country.
Reference Study ID Number: AL46650 https://forpatients.roche.com/ No attachments to email below. contact
Fastest response: use the inquiry form. www.gene.com/contact-us/submit-medical-inquiry contact
United States1 site
- Available
Billings Clinic
Billings, Montana, 59101
Mykola Onyshchenko, Doctor
About this study
Official title: A Multicenter, Open-Label, Expanded Access Program to Provide Divarasib to Patients With Previously Treated KRAS G12c-Positive Advanced or Metastatic Non-Small Cell Lung Cancer
The purpose of this expanded access program (EAP) is to provide early access to divarasib to participants with KRAS G12C-positive (KRAS G12C+) advanced or metastatic non-small cell lung cancer (NSCLC), prior to divarasib becoming commercially available in the United States.
- Conditions
- Non-Small Cell Lung Cancer
- Being tested
- Divarasib
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DivarasibDrug
Also called RO7435846
Participants will self-administer divarasib as per the schedule in the protocol.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-Small Cell Lung CancerStudies of the same condition, open and under way.
- More trials run by Genentech, Inc.The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Expanded access
Sponsor and investigators
- Lead sponsor
- Genentech, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07783009
- Sponsor's protocol ID
- AL46650
- Status last verified
- Oct 2026
- First submitted
- 18 Aug 2026
- Last updated
- 9 Oct 2026
- Results posted
- No