What is LUMAKRAS®?
LUMAKRAS® is a prescription medicine used to treat adults with non-small cell lung cancer (NSCLC) that has spread to other parts of the body or cannot be removed by surgery, and whose tumor has an abnormal KRAS G12C gene, and who have received at least one prior treatment for their cancer.
Your healthcare provider will perform a test to make sure that LUMAKRAS® is right for you. It is not known if LUMAKRAS® is safe and effective in children.
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LUMAKRAS® recommended once-daily, starting dosage: 960 mg orally2
LUMAKRAS® 240 mg tablets have a yellow color. They come in one bottle containing 120 tablets.
Please make sure you take the right number of tablets.2 LUMAKRAS® tablets are comparable in size to a dime.3 Speak with your doctor if you have any questions or if you experience a side effect.
Place your prescribed dose of LUMAKRAS® in a glass of 4 ounces (120 mL) of non-carbonated, room temperature water. Do not crush the tablets. Do not use liquids other than water
Stir or swirl the cup for about 3 minutes until the tablets have broken down into small pieces. They will not completely dissolve. Drink immediately or within 2 hours. The appearance of the mixture may range from pale yellow to bright yellow
Swallow the broken-down tablet mixture. Do not chew pieces of the tablet
Rinse the glass with an additional 4 ounces (120 mL) of water and drink
If the mixture is not consumed immediately, stir or swirl the mixture again to ensure the tablets are mixed into the water and drink
If you take an antacid medicine, such as Tums®, take LUMAKRAS® either 4 hours before or 10 hours after the antacid. Speak to your doctor if you are on a proton pump inhibitor like Prilosec®, or an H2 blocker like Pepcid AC®1
If you miss a dose of LUMAKRAS®, take the dose as soon as you remember. If it has been more than 6 hours, do not take the dose. Take your next dose at your regularly scheduled time the next day. Do not take 2 doses at the same time to make up for a missed dose1
If you vomit after taking a dose of LUMAKRAS®, do not take an extra dose. Take your next dose at your regularly scheduled time the next day1
Patient story represents individual’s experience with LUMAKRAS®. Results may vary.
What should I tell my healthcare provider before taking LUMAKRAS®?
LUMAKRAS® may cause serious side effects, including:
The most common side effects
What is LUMAKRAS®?
LUMAKRAS® is a prescription medicine used to treat adults with non-small cell lung cancer (NSCLC) that has spread to other parts of the body or cannot be removed by surgery, and whose tumor has an abnormal KRAS G12C gene, and who have received at least one prior treatment for their cancer. Your healthcare provider will perform a test to make sure that LUMAKRAS® is right for you. It is not known if LUMAKRAS® is safe and effective in children.
Please see LUMAKRAS® full Prescribing Information.
References: 1. NCI Dictionary of Cancer Terms. www.cancer.gov. Accessed January 27, 2025. 2. LUMAKRAS® (sotorasib) prescribing information, Amgen. 3. Ryan MB, et al. Nat Rev Clin Oncol. 2018;15:709-720. 4. Hong DS, et al. N Engl J Med. 2020;383:1207-1217. 5. Data on file, Amgen; [Analysis of AACR Genie v12].
References: 1. Hong DS, et al. N Engl J Med. 2020;383:1207-1217. 2. NCI Dictionary of Cancer Terms. www.cancer.gov. Accessed January 27, 2025. 3. LUMAKRAS® (sotorasib) prescribing information, Amgen. 4. Sotorasib CSR. Amgen; 2021. 5. Data on file, Amgen; [KRAS G12C Trials Sites]. 6. LUMAKRAS® (sotorasib) patient information, Amgen.
References: 1. LUMAKRAS® (sotorasib) patient information, Amgen. 2. LUMAKRAS® (sotorasib) prescribing information, Amgen. 3. Data on file, Amgen; [Sotorasib Tablet Size].
What should I tell my healthcare provider before taking LUMAKRAS®?