GSK reveals positive but lackluster data from the Ph2b B-Together study (bepirovirsen + pegIFN) in AASLD 2023 abstract
					AASLD 2023 abstracts were released on October 10th, 2023.
GSK presents an oral abstract that will highlight results from the Ph2b B-Together study (bepirovirsen + pegIFN, N=108).
Key Highlights of the Oral Abstract
- The Ph2b B-Together study (N=108) was an open label study where patients received 300mg of bepirovirsen (bepi) (SC Q1W) for 12 wks or 24 wks and then received pegIFN for 24 wks
 - Serious adverse events were experienced by 8 pts (7%), however no new safety signals were observed for bepi
 - Efficacy results were:
 
CI Assessment
- This is the first look of bepi activity in combination with another component required for potential functional cure of 30%
- Data from this study demonstrates lackluster functional cure rates and limited additive benefit of pegIFN when compared to results from B-CLEAR bepi monotherapy study, which demonstrated ~9% functional cure rate
 - Recall, VIR-2218 + peg-IFN demonstrated a SVR24 was 16.1% (5/31)
 
 - This data supports the notion that ASOs in combination therapies can achieve a durable response in HBV but addition of a third component is likely needed
- GSK is currently conducting a Ph2b study evaluating bepi in combination with a vaccine (N=184); data from this study is expected to readout in H1 2026
 - GSK is the only competitor in HBVCure who has all three components to potentially achieve functional cure, however, GSK is yet to initiate a clinical trial with three components
 
 - If GSK continues to develop the bepi + pegIFN combination, an approval as early as 2028 would be possible following the successful completion of a Ph3 study
- If bepi monotherapy is approved (~2026), bepi could be combined with Peg-IFN off-label before approval of the combo
 
 
In addition to this abstract, GSK will also present 8 other abstracts for HBV including 2 post-hoc analyses from Ph2b B-Together study. The post-hoc analyses explore the responses of different HBV genotypes to bepi + pegIFN and mechanistic PK/PD modelling and simulation to inform Ph3 study design. More details on the HBV abstracts from GSK can be found in the table below.
HBV portfolio
| 
 Component  | 
 Molecule and MOA  | 
 Phase of study of monotherapy  | 
| 
 RNA interference molecule  | 
 Bepirovirsen/GSK3228836 (Antisense oligonucleotide)  | 
|
| 
 Vaccine  | 
 GSK3528869A (therapeutic viral vaccine with adjuvanted recombinant protein)  | 
|
| 
 Immune modulator  | 
 GSK5251738 (TLR8 Agonist)  | 
 Ph1 (Study conducted by Shanghai Zhimeng Biopharma)  | 
Other GSK HBV studies:
| 
 Study name  | 
 Combinations of interest  | 
 Phase  | 
 Enrollment  | 
 Data Readout  | 
Potential Approval | Comments | 
| 
 B-WELL 1 B-WELL 2  | 
 ASO monotherapy  | 
 2 x 900  | 
 2H 2025  | 
 Mid-2026  | 
 
  | 
|
| 
 B-TOGETHER  | 
 ASO + Peg-IFNα + NUC  | 
 108  | 
 2H 2023  | 
 H1 2028  | 
 
  | 
|
| 
 -  | 
 ASO + VAX + NUC  | 
 184  | 
 1H 2026  | 
 H1 2031  | 
 
  | 
|
| 
 B-FINE  | 
 ASO monotherapy  | 
 20  | 
 Q1 2024  | 
 -  | 
 Study includes repeat fine needle aspirations of the liver for intrahepatic immunophenotyping  | 
|
| 
 B-SURE  | 
 ASO monotherapy  | 
 450  | 
 Q2 2026  | 
 -  | 
 Long-term follow-up study to assess durability of SVR in bepirovirsen-treated patients; Initial data presented at EASL 2023  | 
|
| 
 B-ASSURED  | 
 ASO monotherapy  | 
 24  | 
 2H 2023  | 
 -  | 
 Investigates pharmacokinetics in cirrhotic patients  | 
|
| 
 -  | 
 ASO + PAPD5/PAPD7 inhibitor  | 
 132  | 
 1H 2026  | 
 Beyond 2032  | 
 PAPD5/7 inhibitors demonstrate neurotoxicity in patients  |