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Efficacy and Safety of Low-dose Ibrutinib and Itraconazole in Chronic Graft Versus Host Disease

Sponsored by Hospital Universitario Dr. Jose E. Gonzalez

About this trial

Last updated 3 years ago

Study ID

PI22-00027

Status

Unknown status

Type

Interventional

Phase

Phase 2

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 years ago

What is this trial about?

Chronic graft-versus-host disease (cGVHD) affects 30 to 70% of Allogeneic Hematopoietic Cell Transplantation, decreases the quality of life, and increases mortality. First-line treatments for cGVHD are steroids, however, up to 50% of patients do not respond to treatment. There is no well-defined second-line treatment for cGVHD, but ibrutinib, a Bruton tyrosine kinase inhibitor, has been successfully used in phase 2 clinical trials for moderate to severe steroid-refractory cGVHD and has been shown to be safe, showing rates of response of 69% at a median follow-up of 26 months. Therefore, ibrutinib was approved by the FDA for the treatment of steroid-refractory cGVHD. Also, it is known that ibrutinib is metabolized by cytochrome isoenzyme 3A4 and that itraconazole is a potent inhibitor of this hepatic isoenzyme. Therefore, the investigators hypothesized that in subjects with newly diagnosed cGVHD and in patients with steroid-refractory cGVHD, low-dose ibrutinib in combination with itraconazole might be effective and safe.

What are the participation requirements?

Yes

Inclusion Criteria

- Age (>18 years)

- Any type of peripheral blood stem cell transplant (matched-related, match non-related, and haplo)

- Any conditioning regimen

- Newly diagnosed moderate to severe chronic graft versus host disease

- Steroid refractory moderate to severe chronic graft versus host disease defined as progression with prednisone 1mg/kg/day, or stable disease after four to six weeks of prednisone >0.5 mg/kg/day, or disease progression when reducing prednisone below <0.5 mg/kg/día.

5. Eastern Cooperative Oncology Group (ECOG) <= 2
No

Exclusion Criteria

- Disease relapse (excluding positive minimal residual disease)

- Secondary malignancies

- Disease progression

- Use of B lymphocyte cytotoxics in the last month (i.e., rituximab, bortezomib)

- Advance stages of heart failure (NYHA III o IV)

- Ventricular arrhythmias

- Uncontrolled hypertension

- Ischemic heart diseases such as unstable angina or stable angina in the last six months

- Hepatitis B or C

- Hypersensitivity to ibrutinib

- Active bleeding

- Uncontrolled acute infection

- Hepatopathy Child-Pugh C

- Pregnancy

Locations

Location

Status

Recruiting