⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Study of Lenalidomide/Ixazomib/Dexamethasone/Daratumumab in Transplant-Ineligible Patients With Newly Diagnosed MM

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study of Lenalidomide/Ixazomib/Dexamethasone/Daratumumab in Transplant-Ineligible Patients With Newly Diagnosed MM

Official Title: A Phase II Study of Lenalidomide, Ixazomib, Dexamethasone, and Daratumumab in Transplant-Ineligible Patients With Newly Diagnosed Multiple Myeloma

Study ID: NCT04009109

Study Description

Brief Summary: A randomized Phase II clinical trial will be conducted to assess the impact on progression free survival (PFS) with the addition of ixazomib and daratumumab to lenalidomide as a maintenance treatment following induction with lenalidomide, ixazomib, dexamethasone, and daratumumab. Patients will be randomized to either: Arm A: 12 cycles of lenalidomide, ixazomib, daratumumab, and dexamethasone followed by lenalidomide until disease progression or unacceptable toxicity or a maximum of 2 years of maintenance therapy. Arm B: 12 cycles of lenalidomide, ixazomib, daratumumab and dexamethasone, followed by lenalidomide, ixazomib, and daratumumab until disease progression or unacceptable toxicity or a maximum of 2 years maintenance therapy.

Detailed Description: Induction Phase: 28-day treatment cycle. Treatment continues until disease progression or for a maximum of 12 cycles as follows: Cycles 1-2: * Lenalidomide - 15 mg PO QD on Days 1-21 * Ixazomib - 4 mg PO on Days 1, 8, 15 * Daratumumab Subcutaneous - 15mL/1800mg on Days 1, 8, 15, 22 * Dexamethasone - 20 mg PO on Days 1, 2, 8, 9, 15, 16, 22, 23; For participants ≥75, dexamethasone administered on days 1, 8, 15, 22 Cycles 3-6: * Lenalidomide - 15 mg PO QD on Days 1-21 * Ixazomib - 4 mg PO on Days 1, 8, 15 * Daratumumab Subcutaneous - 15mL/1800mg on Days 1, 15 * Dexamethasone - 20 mg PO on Days 1, 2, 8, 9, 15, 16; For participants ≥75, dexamethasone administered on days 1, 8, 15 Cycles 7-12: * Lenalidomide - 15 mg PO QD on Days 1-21 * Ixazomib - 4 mg PO on Days 1, 8, 15 * Daratumumab Subcutaneous - 15mL/1800mg on Day 1 * Dexamethasone - 20 mg PO on Days 1, 2, 8, 9, 15, 16; For participants ≥75, dexamethasone administered on days 1, 8, 15 Maintenance Phase: 28-day treatment cycle. Treatment continues until progression or a maximum of 2 years of maintenance treatment: Arm A • Lenalidomide - 10 mg PO QD on Days 1-21 Arm B * Lenalidomide - 10 mg PO QD on Days 1-21 * Ixazomib - 3 mg (or last tolerated dose from the induction phase) PO on Days 1, 8, and 15 * Daratumumab Subcutaneous - 15mL/1800mg on Day 1 * Dexamethasone - 20mg PO on Day 1; Unless patient is ≥75 then 10mg po day 1 In the maintenance phase, dexamethasone, 20 mg PO orally or IV will be administered to patients as a pre-infusion medication prior to daratumumab dosing. When dexamethasone is reduced to 20 mg/week and is given as pre-infusion medication, patients may receive low-dose methylprednisolone (≤20 mg) orally (or equivalent in accordance with local standards) for the prevention of delayed IRRs as clinically indicated. If the investigator wishes to continue the maintenance regimen at the end of the 2 years maintenance treatment, patients may continue current maintenance as per standard of care.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Northern Light Eastern Maine Medical Center, Bangor, Maine, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

University of Nebraska Medical Center, Omaha, Nebraska, United States

SUNY Upstate Medical Center, Syracuse, New York, United States

University of North Carolina, Chapel Hill, North Carolina, United States

Gibbs Cancer Center & Research Institute/Spartanburg Regional Healthcare, Spartanburg, South Carolina, United States

Contact Details

Name: Evanthia Galanis, MD

Affiliation: Alliance Foundation Trials, LLC.

Role: PRINCIPAL_INVESTIGATOR

Name: Andrew Yee, MD

Affiliation: Massachusetts General Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: