BGJ398 in Non-Muscle-Invasive Urothelial Carcinoma of the Bladder

Completed · Not applicable

Conditions studied: Bladder Cancer, Non-Muscle-Invasive Urothelial Carcinoma

In brief

The purpose of this study is to study the activity and effects of BGJ398 on bladder cancer tumors that are confined to the lining of the bladder.

Key facts

Study ID

NCT02657486

Run by

Memorial Sloan Kettering Cancer Center

People needed

4

Starts

2016-01-06

Expected to finish

2026-02-04

Last updated by the study team

2026-02-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Recurrent high-risk non-muscle-invasive bladder cancer after prior intravesical BCG therapy meeting all of the following criteria:
• Histologically documented diagnosis of urothelial carcinoma confirmed by the Department of Pathology at MSKCC.
• Documentation of activating FGFR3 mutation or gene fusion on an assay performed in a CLIA-certified laboratory.
• History of high-grade, non-muscle-invasive bladder cancer (NMIBC).
• Clinical evidence of high-grade, stage pTa NMIBC.
• Prior intravesical therapy with at least one induction course of BCG
• Multiple papillary lesions with at least one amenable to marker tumor study (≤1 cm, non-invasive; or could be partially resected to leave a non-invasive lesion ≤1 cm) OR solitary papillary lesion amenable to marker tumor study (≤1 cm, non-invasive)
• Patient must be willing to consent to MSKCC protocol 12-245 ("Tumor Genomic Profiling in Patients Evaluated for Targeted Cancer Therapy"
• Age 18 years or older.
• Patient must be willing and able to comply with scheduled visits, treatment plan, and laboratory tests.
• Patient must be able to swallow and retain oral medication.
• Karnofsky performance status of ≥80.
• Recovery from adverse events of previous systemic anti-cancer therapies to baseline or grade 1, except for:
• Alopecia
• Stable neuropathy of ≤ grade 2 due to prior cancer therapy
• Women of childbearing potential, defined as all women physiologically capable of becoming pregnant, must agree to use highly effective methods of contraception during dosing and for 3 months following the discontinuation of study treatment.
• Highly effective contraception methods include:
• Total abstinence (when this is in line with the preferred and usual lifestyle of the subject). Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
• Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow-up hormone level assessment.
• Male sterilization (at least 6 months prior to screening). For female subjects the vasectomized male partner should be the sole partner.
• Combination of any two of the following (a+b, a+c, or b+c):
• Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate <1%); for example, hormone vaginal ring or transdermal hormone contraception.
• Placement of an intrauterine device (IUD) or intrauterine system (IUS)
• Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository.
• Oral contraceptives (OC), injected or implanted hormonal methods are not allowed as the sole method of contraception because BGJ398 has not been characterized with respect to the potential to interfere with PK and/or the effectiveness of OCs.

You may not qualify if…

• Clinical suspicion of active CIS.
• Evidence of >1 area of CIS not associated with papillary tumor at this time.
• Evidence of >7 tumors present in the bladder.
• History or evidence of advanced urothelial carcinoma, including enlarged lymph nodes and/or distant metastases.
• Evidence of upper tract urothelial carcinoma.
• History of another primary malignancy within the last 3 years except:
• Adequately treated in situ carcinoma of the cervix
• Non-melanoma carcinoma of the skin
• Any other curatively treated malignancy that has not been treated in the prior 3 months and is not expected to require treatment for recurrence during the course of the study.
• Patients who received prior treatment with a selective FGFR inhibitor.
• Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of oral BGJ398 (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, small bowel resection).
• History and/or current evidence of tissue calcification including, but not limited to, the soft tissue, kidneys, intestine, myocardium, and lung with the exception of calcified lymph nodes and asymptomatic vascular calcification.
• Current evidence of endocrine alterations of calcium/phosphate homeostasis, e.g., parathyroid disorders, history of parathyroidectomy, tumor lysis, tumoral calcinosis, etc.
• Use of medications that increase serum levels of phosphorus and/or calcium (e.g., calcium, phosphate, vitamin D, parathyroid hormone;) .
• Current evidence of corneal or retinal disorder/keratopathy including, but not limited to, bullous/band keratopathy, corneal abrasion, inflammation/ulceration, and/or keratoconjunctivitis, confirmed by ophthalmologic examination
• Treatment with any of the following anti-cancer therapies prior to the first dose of BGJ398 within the stated timeframes:
• Cyclical chemotherapy (intravenous) within a period of time that is shorter than the cycle length used for that treatment (e.g., 6 weeks for nitrosourea, mitomycin-C).
• Biological therapy (e.g., antibodies - including bevacizumab) within a period of time that is ≤ 5 half-lives or ≤ 4 weeks, whichever is shorter, prior to starting study drug.
• Continuous or intermittent small molecule therapeutics within a period of time that is ≤ 5 half-lives or ≤ 4 weeks (whichever is shorter) prior to starting study drug.
• Any other investigational agents within a period of time that is ≤ 5 half-lives or less than the cycle length used for that treatment or ≤ 4 weeks (whichever is shortest) prior to starting study drug.
• Wide field radiotherapy (including therapeutic radioisotopes such as strontium 89) ≤ 4 weeks or limited field radiation for palliation ≤ 2 weeks prior to starting study drug.
• Patients who are currently receiving treatment with agents that are known strong inducers or inhibitors of CYP3A4
• Consumption of grapefruit, grapefruit juice, grapefruit hybrids, pomelos, pomegranates, star fruits, Seville oranges or related products within 7 days prior to first dose
• Use of herbal preparations/medications (including, but not limited to: St. John's wort, Kava, ephedra (ma huang), gingko bilboa, dehydroepiandrosterone (DHEA), yohimbe, saw palmetto, and ginseng within 7 days prior to first dose.
• Use of medications that are known to prolong the QT interval and/or are associated with a risk of Torsades de Pointes 7 days prior to first dose

Where it is running

• Memorial Sloan Kettering Cancer Center — New York, New York, United States

Full record on ClinicalTrials.gov

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