Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04502030 · ClinicalTrials.gov registry record · Phase 3

Double-blind, Randomized, Placebo-controlled, Prospective Phase III Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients With Chronic Lymphocytic Leukemia ("PRO-SID" Study)

A Phase 3 study, sponsored by Octapharma.

Completed
Registry status
Phase 3
Development phase
247
Enrollment target

NCT04502030: Completed Phase 3 study, sponsored by Octapharma.

NCT04502030 is a Phase 3 study that has completed, run by Octapharma. The registered enrollment target is 247 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04502030, a Phase 3 study, has completed, sponsored by Octapharma.

COMPLETED
Registry status
Phase 3
Development phase
247 participants
Enrollment target

Study Summary

Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients with Chronic Lymphocytic Leukemia

Primary Outcome

Major infection for this trial is defined as: * Bacterial and/or viral infections resulting in death * Bacterial and/or viral infections, which are microbiologically documented (MDI) or clinically documented (CDI) requiring treatment with anti-infectives; upper respiratory tract infections, bronchitis, lower urinary tract infections, localized skin infections and stomatitis (MDI or CDI) are considered major only if they require treatment with antiinfectives AND hospitalization or hospitalizatio

Interventions

  • OTHER Placebo
  • BIOLOGICAL Panzyga

Trial Details

FieldValue
Enrollment Target 247 participants
Start Date 2020-10-05
Est. Completion 2025-09-19
Phase Phase 3
Octapharma

43 total trials

What the finished NCT04502030 record still lists

NCT04502030 is an interventional study that assigns participants to a tested intervention. The registered 247 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04502030 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04502030 about?

NCT04502030 is a clinical study titled "Double-blind, Randomized, Placebo-controlled, Prospective Phase III Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients With Chronic Lymphocytic Leukemia ("PRO-SID" Study)". Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients with Chronic Lymphocytic Leukemia

What is the current status of trial NCT04502030?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 247 participants. The study started on 2020-10-05. Estimated completion is 2025-09-19.

What interventions are being tested in trial NCT04502030?

The interventions under investigation include: Placebo (OTHER), Panzyga (BIOLOGICAL).

Who is sponsoring clinical trial NCT04502030?

This trial is sponsored by Octapharma, which has 43 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04502030's enrollment target sits among peer trials

247 1266th of 2000 higher than 734 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04269902 · 247 participants · Phase 3

    Testing Early Treatment for Patients With High-Risk Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Leukemia (SLL), EVOLVE CLL/SLL Study

  • NCT04989803 · 247 participants · Phase 1

    Study of KITE-363 or KITE-753 in Participants With Relapsed and/or Refractory B-cell Lymphoma

  • NCT05521399 · 247 participants

    Heart Transplantation - Renewal

  • NCT05556824 · 247 participants · Phase 2

    Multi-Center Study of Panosyl-Isomaltooligosaccharides Adjunctive to PPI Therapy to Treat GERD

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04502030, the US trial registry maintained by the National Library of Medicine. NCT04502030 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.