NO_LONGER_AVAILABLENot Applicable

Expanded Access to TAK-113 for Adults With Metastatic Colorectal Cancer (mCRC)

Plain-language summary

The expanded access program allows people to gain access to an unlicensed treatment on compassionate grounds. This expanded access program provides adults with refractory metastatic colorectal cancer (mCRC) and who cannot neither adequately be treated by current standard of care nor participate in a clinical study access to TAK-113 until TAK-113 becomes commercially available in the respective country or the adult does no longer seem to benefit from treatment with TAK-113.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Eastern Cooperative Oncology Group (ECOG) physical status of 0-2.
✓. Histologically and/or cytologically documented metastatic colorectal adenocarcinoma.
✓. Received all locally available and appropriate prior standard therapies and no other satisfactory treatment option is available for this condition. Participants may have received either prior TAS-102 or regorafenib. Must have progressed on or intolerant to fluoropyrimidine-, oxaliplatin-, and irinotecan- based chemotherapies, anti-vascular endothelial growth factor (VEGF) therapy, and, if rat sarcoma (RAS) wild-type, an anti- epidermal growth factor receptor (EGFR) therapy if available locally for this condition.
✓. Adequate bone marrow and organ function as defined by the following:
✓. Absolute neutrophil count of ≥1.5×10\^9 per liter, platelet count of ≥75×10\^9 per liter, and hemoglobin ≥8 grams per deciliter (g/dL).
✓. Serum total bilirubin ≤1.5 times the upper limit of normal (ULN)
✓. Urine dipstick ≤1+ for proteinuria or ≤30 milligrams per deciliter (mg/dL) in urinalysis, unless quantitative protein is \<1000 milligram (mg) in a 24-hour urine sample or urine protein: creatinine ratio on spot urine testing is ≤1.9.
✓. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), or alkaline phosphatase levels ≤2.5 times the ULN (participants with liver metastases must have ALT and AST levels ≤5 times the ULN).

Exclusion criteria

✕. Received systemic anticancer therapies \[including chemotherapy, tyrosine-kinase inhibitors (TKIs) and endocrine therapy\] within 2 weeks prior to the first dose of study drug.
✕. Uncontrolled hypertension as defined per local institution.
✕. Any unresolved toxicities from a previous antitumor treatment greater than National Cancer Institute (NCI) Common Terminology Criteria for Adverse Event (CTCAE) version 5.0 grade 1 (except for alopecia or neurotoxicity grade≤2).
✕. Major surgery within the last 60 days or have had any other minor surgery or invasive procedure within the last 4 weeks.
✕. Any thromboembolic events (including deep vein thrombosis, and pulmonary embolism) within the past 6 months, or history of stroke and/or transient ischemic attack within the last 12 months.

Trial details

NCT IDNCT06195514

SponsorTakeda

Sponsor typeINDUSTRY

Study typeEXPANDED_ACCESS

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