306 Participants NeededMy employer runs this trial

Rocbrutinib vs Pirtobrutinib for Chronic Lymphocytic Leukemia

Recruiting at 5 trial locations
AY
SA
Overseen ByStephen Anthony, D.O.
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Newave Pharmaceutical Inc
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial compares two treatments, rocbrutinib and pirtobrutinib, for individuals with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who have not responded to previous treatments. The main goal is to determine which treatment prolongs life without disease progression. Individuals with CLL or SLL who have previously tried a Bruton's tyrosine kinase inhibitor and require further treatment may be suitable candidates for this trial. Participants will take either rocbrutinib or pirtobrutinib daily and will be monitored for treatment effectiveness and impact on quality of life. As a Phase 3 trial, this study represents the final step before FDA approval, providing participants with access to potentially groundbreaking treatments.

Do I have to stop taking my current medications for the trial?

The trial protocol does not specify if you must stop taking your current medications, but it mentions that certain medications or conditions that pose a strong drug-drug interaction risk are prohibited. It's best to discuss your current medications with the trial team to see if any adjustments are needed.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Earlier studies have shown that rocbrutinib is safe for patients with chronic lymphocytic leukemia (CLL). Patients generally tolerate it well, even those who have tried similar treatments. Some experienced mild side effects, but these were not severe enough to discontinue the medication.

Research on pirtobrutinib also indicates safety. Patients with CLL have used it without major issues, and most side effects were minor and manageable.

Both treatments have undergone thorough study and are considered safe for many patients. However, individual experiences can differ, so discussing any concerns with a doctor is important.12345

Why are researchers excited about this trial's treatments?

Unlike the standard treatments for chronic lymphocytic leukemia, which often include drugs like ibrutinib and acalabrutinib, Rocbrutinib and Pirtobrutinib offer new approaches. Both drugs are designed to target and inhibit Bruton's tyrosine kinase (BTK) but in slightly different ways. Rocbrutinib is particularly exciting because it may offer improved targeting precision, potentially reducing side effects compared to existing therapies. Pirtobrutinib is a non-covalent BTK inhibitor, allowing it to bind effectively even in the presence of certain genetic mutations that can make other treatments less effective. Researchers are optimistic that these treatments could provide patients with more personalized and effective options.

What evidence suggests that this trial's treatments could be effective for chronic lymphocytic leukemia?

This trial will compare Rocbrutinib and Pirtobrutinib for treating chronic lymphocytic leukemia (CLL). Research has shown that Rocbrutinib, one of the treatments in this trial, yields promising results for patients with CLL who have previously tried similar treatments. Specifically, one study found that 69% of these patients did not experience disease progression after 18 months, particularly when starting with higher doses. Meanwhile, Pirtobrutinib, the other treatment option in this trial, has demonstrated high effectiveness, with studies showing an 87% response rate, comparable to ibrutinib, a well-known treatment. Both Rocbrutinib and Pirtobrutinib are proving effective in managing CLL, offering hope for patients who have tried other options.12678

Are You a Good Fit for This Trial?

This trial is for adults (18+) with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) whose disease has come back or not responded to treatment, and who have already tried a covalent BTK inhibitor. Participants must be well enough to do daily activities and have good organ function.

Inclusion Criteria

My cancer has a confirmed 17p deletion.
I am 18 years old or older.
My CLL/SLL diagnosis is confirmed by lab tests.
See 6 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive rocbrutinib or pirtobrutinib continuously in 28-day cycles until disease progression or unacceptable toxicity

Up to approximately 4 years
Monthly visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

Open-label extension (optional)

Participants may opt into continuation of treatment long-term

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • Pirtobrutinib
  • Rocbrutinib

Trial Overview

The study compares two oral drugs, rocbrutinib and pirtobrutinib, taken once daily in cycles. Patients are randomly assigned to one of the two treatments to see which works better at controlling CLL/SLL after previous therapies.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: RocbrutinibExperimental Treatment1 Intervention
Group II: PirtobrutinibActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Newave Pharmaceutical Inc

Lead Sponsor

Trials
4
Recruited
270+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/41749915/

Efficacy of Pirtobrutinib Monotherapy in Treatment-Naïve ...

Conclusions: This NMA shows that pirtobrutinib has better PFS outcomes than ibrutinib. While PFS outcomes suggest that pirtobrutinib is ...

The efficacy and safety of pirtobrutinib in patients with CLL/SLL

Pirtobrutinib, a highly selective, non-covalent BTKi, has demonstrated promising efficacy and a favorable safety profile in patients with CLL/ ...

Pirtobrutinib after a Covalent BTK Inhibitor in Chronic ...

In this trial, pirtobrutinib showed efficacy in patients with heavily pretreated CLL or SLL who had received a covalent BTK inhibitor.

Pirtobrutinib Versus Ibrutinib for Treating CLL

Pirtobrutinib was just as effective as ibrutinib (non-inferior), with an overall response rate of 87% compared with 79% for ibrutinib for all ...

Pirtobrutinib Yields Improved Survival Outcomes in ...

Key Points: In the phase 3 BRUIN CLL-321 trial, pirtobrutinib demonstrated improved progression-free survival (PFS) and time to next ...

Pirtobrutinib in Chronic Lymphocytic Leukemia - PMC - NIH

Data derived from the BRUIN CLL-321 clinical trial indicate that pirtobrutinib achieves a median TTNT of approximately 2.5 years in patients who are naïve to ...

Comparative Data, Safety Profiles, and Sequencing with ...

Experts discuss the implications of recent studies on pirtobrutinib, comparing its efficacy and safety against other BTK inhibitors for CLL ...

Pirtobrutinib Outperforms Bendamustine Plus Rituximab for ...

Researchers said that the results suggest pirtobrutinib has strong potential as a first-line treatment for CLL/SLL. However, the study used a ...