Search
Close this search box.

CAR T cells in lupus: Promising results at EULAR 2024 and emergence of China

At the recent European Alliance of Associations for Rheumatology (EULAR) 2024 conference, chimeric antigen receptor (CAR) T-cell modalities in autoimmune diseases, including systemic lupus erythematosus (SLE) and lupus nephritis (LN), was featured as a key topic.

This modality’s potential to achieve drug-free remission in patients with autoimmune diseases such as SLE and LN is a key focus that pharma companies continue to explore.

The results presented at EULAR 2024 from ongoing, industry-sponsored, early-stage clinical trials generally gave early indications that CAR T-cell assets may be able to achieve an immune reset and potentially help patients achieve drug-free remission.

However, reports of relapse post-infusion have drawn cautious optimism about an otherwise promising display of results for CAR T-cell assets in this disease space.

Achieving drug-free remission would represent a transformative, paradigm-shifting moment in the care of patients with SLE and LN.

Results from ongoing clinical trials indicate a movement in the right direction for CAR T-cell assets in SLE and LN.

Access the most comprehensive Company Profiles
on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free
sample

Your download email will arrive shortly

We are confident about the
unique
quality of our Company Profiles. However, we want you to make the most
beneficial
decision for your business, so we offer a free sample that you can download by
submitting the below form

By GlobalData

<!–

–>

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Kyverna Therapeutics’ KYV-101 exhibited disease control at a follow-up period, with six of the seven patients with LN not requiring immunosuppressants and two of these patients having completed at least six months post-infusion.

Results from Cabaletta Bio’s CABA-201 RESET-SLE trial indicated an improvement in the SLE Disease Activity Index 2000 score and resolution of vasculitis, arthritis, and haematuria within four weeks post-infusion in one patient with SLE, with ongoing taper from prednisone 10mg per day.

Preliminary data from JW Therapeutics’ JWCAR029 also suggested efficacy, with three patients in the low-dose group showing a reduction in Safety of Estrogens in Lupus Erythematosus National Assessment–SLEDAI scores at four months follow-up.

Additionally, all three patients achieved SLE responder index-4 while two patients reached lupus low disease activity status.

iCell Gene Therapeutics’ BCMA CD19 compound CAR T cells also delivered promising results that demonstrated SLE patients free of lupus medication at a mean follow-up period of 20 months and in LN patients at a mean follow-up period of 16 months.

While the general sentiment over these results has been positive, episodes of relapses among patients have generated caution, including in the case of one patient who received KYV-101 and relapsed five months post-infusion.

According to leading data and analytics company GlobalData’s Pharmaceutical Intelligence Center, of the 18 CAR T-cell assets currently in pipeline clinical development for SLE/LN, 50% of pipeline assets are being evaluated in China (Table 1).

This trend indicates the emergence of China as a leader in the development of CAR T-cell therapies within the autoimmune disease space.

The trend also highlights the opportunity for large pharma companies to partner with companies conducting clinical trials in China to propel the growth of the CAR T-cell modality on a broader geographical scale.

Clinical developments and commercial partnerships within the CAR T-cell space will be crucial to meet the unmet needs that exist within the SLE and LN disease spaces.

Key opinion leaders interviewed by GlobalData have emphasised the need for agents that can help patients, especially those with refractory forms of the disease, into remission without the need for these patients to be on traditional steroid and immune-suppressive therapies.

As these innovator modalities continue along the path of development, clinical milestones achieved during this process will be seen as key moments that will propel the growth of this market.