LDE225 and Paclitaxel in Solid Tumors

Ovarian Cancer Clinical Trial

Official title:

LDE225 in Combination With Paclitaxel in Patients With Advanced Solid Tumors - A Multicenter Phase I Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01954355
• Other study ID #: SAKK 65/12
• Secondary ID: CLDE225XCH01T201
• Status: Completed
• Phase: Phase 1
• Start date: September 2013
• Est. completion date: November 2016

Study information

• Verified date: December 2019
• Source: Swiss Group for Clinical Cancer Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary aim of this trial is to establish the maximum tolerated dose (MTD) and the recommended phase II dose (RP2D) of LDE225 given in combination with standard doses of paclitaxel in patients with advanced solid tumors. In addition, the preliminary anti-tumor activity of this combination will be assessed, in particular in ovarian cancer.

Description:

This is a multicenter, open label phase I dose-escalation trial of LDE225 administered once daily (OD) with Paclitaxel administered weekly for three weeks (days 1, 8, 15) in 28-day cycles in adult patients with advanced solid tumors that have progressed despite standard therapy.

The trial will consist of three parts. In Part A (dose escalation following a standard 3+3 design), patients with previously treated advanced solid tumors will receive escalating doses of LDE225 in combination with standard Paclitaxel doses, to define the MTD and the RP2D of LED225 OD that can be given in combination with standard doses of Paclitaxel. Once the MTD and RP2D is established in 6 patients, then part B will start.

Part B and C are expansion cohorts in patients with advanced platinum-resistant ovarian cancer (6 patients each) to further evaluate the safety of the combination and to assess for any preliminary antitumor activity.

In Part B, any prior taxane therapy must have been administered on a 3-week schedule. In Part C, prior taxane therapy must have been administered on weekly schedule and has to be followed by a wash-out period of at least 6 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: November 2016
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient must give written informed consent before registration.

• For Part A: Histologically or cytologically confirmed diagnosis of advanced solid tumors that have progressed despite standard therapy. No more than two prior lines of chemotherapy for advanced disease.

• For Part B: Histologically or cytologically confirmed diagnosis of advanced ovarian cancer. Prior chemotherapy must have contained a platinum and a taxane at some point. Any prior taxane therapy must have been administered on a 3-week schedule. A maximum of 2 prior chemotherapy lines for advanced disease will be permitted. Patients must be refractory (PD during chemotherapy) or resistant (PD within 6 months of completing chemotherapy) to their last platinum-containing chemotherapy regimen.

• For Part C: Histologically or cytologically confirmed diagnosis of advanced ovarian cancer. Prior chemotherapy must have contained a platinum and a taxane at some point. Prior taxane therapy must have been administered on weekly schedule and must be followed by a wash-out period of at least 6 months. A maximum of 2 prior chemotherapy lines for advanced disease will be permitted. Patients must be refractory (PD during chemotherapy) or resistant (PD within 6 months of completing chemotherapy) to their last platinum-containing chemotherapy regimen.

• For Parts B and C, patients must have measurable disease according to RECIST v1.1 Radiological evaluations to be performed within 4 weeks before registration.

• WHO performance status 0-1

• Age = 18 years

• Hematological values: ANC = 1.5 x 109/L, platelets = 100 x 109/L, Hemoglobin = 100 g/L

• Adequate hepatic function: bilirubin = 1.5 x ULN, AST and ALT = 2.5 x ULN or = 5.0 x ULN if liver metastases are present

• Creatine phosphokinase (CPK) = ULN

• Albumin = 30g/L

• Adequate renal function (calculated creatinine clearance > 50 mL/min, according to the formula of Cockcroft-Gault, see Appendix 3)

• Archived tumor tissue must be available.

• Women are not breastfeeding.

• Women of child-bearing potential are using effective contraception, are not pregnant and agree not to become pregnant during participation in the trial and during the 12 months thereafter. They are required to have a negative serum pregnancy test before registration (within 7 days).

• Men agree not to father a child during participation in the trial and during 12 months thereafter. They agree to use effective contraception.

Exclusion Criteria:

• Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the trial or those who prior to the first dose of combination have not recovered to = CTCAE Grade 1 from adverse events due to agents administered more than 4 weeks earlier

• Symptomatic brain metastases

• Prior therapy with a Hedgehog inhibitor

• Known or prior hypersensitivity to taxanes or drugs containing Cremophor in spite of premedication

• Positive HIV test

• Positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test

• Impairment of gastrointestinal (GI) function or GI disease (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection)

• Impaired cardiac function or clinically significant heart disease

• Patients who are receiving treatment with medications that are known to be strong inhibitors or inducers of CYP3A4/5 or drugs metabolized by CYP2B6 or CYP2C9 that cannot be discontinued

• Patients who are currently receiving treatment with warfarin sodium (Coumadin)

• Patients who are currently receiving immunosuppressive treatment and in whom the treatment cannot be discontinued prior to starting trial drug.

• Patients receiving medications that are recognized to cause rhabdomyolysis, such as HMG CoA reductase inhibitors (statins) clofibrate, gemfibrozil, and that cannot be stopped at least 2 weeks prior to the initiation of LDE225 treatment

• Patients who have undergone major surgery = 2 weeks prior to starting trial drug or who have not recovered from such therapy

• Psychiatric disorder precluding understanding of information on trial related topics, giving informed consent, or interfering with compliance for oral drug intake.

Related Conditions & MeSH terms

• Ovarian Cancer
• Ovarian Neoplasms
• Solid Tumor

Intervention

Drug:
• LDE225
400, 600 and 800 mg OD
• Paclitaxel
80 mg/m2 (days 1, 8, 15)

Locations

Country	Name	City	State
Switzerland	Istituto Oncologico della Svizzera Italiana	Bellinzona
Switzerland	Kantonsspital Graubünden	Chur
Switzerland	Centre Pluridisciplinaire d`Oncologie CHUV	Lausanne
Switzerland	Kantonsspital St. Gallen	St. Gallen

Sponsors (1)

Lead Sponsor	Collaborator
Swiss Group for Clinical Cancer Research

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose limiting toxicities (DLTs) of the combination of LDE225 with paclitaxel in patients with advanced solid tumors		until up to 4 weeks after start of trial therapy
Secondary	Frequency and severity of adverse events based on the Common Terminology Criteria for Adverse Events V.4.0 (CTCAE).		expected average 3 months
Secondary	Objective tumor responses based on RECIST 1.1 criteria.		expected average 3 months