Immunology Pipeline

At GSK, our pipeline is focused on unlocking the science of the immune system, human genetics, and advanced technologies to develop vaccines and specialty medicines.

Our products in development progress through three stages: phase I, phase II, and phase III/registrational. Each of these phases allows us to assess the safety and efficacy of our investigational products to eventually provide data to support applications for regulatory approval.

View our ongoing, innovative research with autoimmune diseases.

Phase 1 Overview

This is the first time a new vaccine or medicine is tested in humans; it will usually be given to a small group of healthy volunteers, or it may be tested on patients who have the condition it is designed to treat. The principal objectives in phase I are to ensure the new vaccine or medicine presents no major safety issues, and to see clear evidence that it can reach the targeted body area and remain there long enough to deliver its potential benefits. We also seek to gain preliminary evidence the vaccine or medicine can offer therapeutic value or help to prevent the disease in question.

DISEASE STATES

 
Systemic Lupus Erythematosus (SLE)

No studies exist in this phase

Eosinophilic Granulomatosis with Polyangiitis (EGPA)
No studies exist in this phase
Systemic Sclerosis

No studies exist in this phase

Phase 2 Overview

At this stage, the potential vaccine or medicine is usually tested to understand the effectiveness against the disease it is designed to treat and appropriate dosing levels. The performance of the medicine in one group of patients may be compared against another group of patients receiving a placebo (a treatment that looks the same as the potential new medicine but has no active ingredients) or an existing treatment.

DISEASE STATES

 
Systemic Lupus Erythematosus (SLE)
Anti-BLyS (Belimumab)

SABLE: Safety and Effectiveness of Belimumab in Systemic Lupus Erythematosus Registry

Eosinophilic Granulomatosis with Polyangiitis (EGPA)

VCRC-VPPRN EGPA Registry (Observational Study)

Systemic Sclerosis

   

A Study of the Efficiency And Safety Study of Belimumab Compared To Placebo In Adults With Systemic Sclerosis Associated Interstitial Lung Disease (BLISSc-ILD)

Phase 3 Overview

This phase consists of a much larger and potentially longer trial, often involving hundreds or possibly thousands of participants from a range of different countries. The principal objectives in phase III are to demonstrate the safety and effectiveness of the new vaccine or medicine in the typical patient likely to use it; confirm effective dosing levels; identify contraindications; build knowledge of the benefits of the vaccine or medicine and compare them with any risks; and compare results against any currently achieved by existing treatments. Regulators will determine how a new product should be used and which patients should qualify for it based on all the evidence from clinical and pre-clinical studies.

DISEASE STATES

 
Systemic Lupus Erythematosus (SLE)
Anti-BLyS (Belimumab)

SABLE: Safety and Effectiveness of Belimumab in Systemic Lupus Erythematosus Registry

A Study Describing the Efficacy and Safety of Belimumab Administered in Adult Participants With Early Systemic Lupus Erythematosus (SLE) (BE-EARLY)

Eosinophilic Granulomatosis with Polyangiitis (EGPA)

VCRC-VPPRN EGPA Registry (Observational Study)

Systemic Sclerosis

   

A Study of the Efficiency And Safety Study of Belimumab Compared To Placebo In Adults With Systemic Sclerosis Associated Interstitial Lung Disease (BLISSc-ILD)