Showing posts with label MAB. Show all posts
Showing posts with label MAB. Show all posts

Friday, June 28, 2019

Lutikizumab in Osteoarthritis


Lutikizumab (ABT-981) is an anti-interleukin-1α/β (anti-IL-1α/β) dual variable domain immunoglobulin. I’ve once discussed bispecific antibodies with Prof. Burmester as I have concerns about the fact that each part is as strong as the other and this might not reflect the need of each compound. Prof. Burmester had a more practical approach as you don’t have to apply for two different drugs in studies and later in looking for approval by agencies such as the FDA or EMA. I remain skeptic.

There has been a study by R.M. Fleischman and colleagues [1]: “A Phase II Trial of Lutikizumab, an Anti-Interleukin-1α/β Dual Variable Domain Immunoglobulin, in Knee Osteoarthritis Patients With Synovitis.” The authors found only a limited improvement in the WOMAC pain score and a lack of synovitis improvement with lutikizumab. The concluded further that “together with published results from trials of other IL-1 inhibitors, suggest that IL-1 inhibition is not an effective analgesic/antiinflammatory therapy in most patients with knee OA and associated synovitis.”

M. Kloppenburg and colleagues published a study [2]: “Phase IIa, placebo-controlled, randomised study of lutikizumab, an anti-interleukin-1α and anti-interleukin-1β dual variable domain immunoglobulin, in patients with erosive hand osteoarthritis.” The had chosen as primary endpoint a “change in Australian/Canadian Osteoarthritis Hand Index (AUSCAN) pain subdomain score from baseline to 16 weeks. At baseline and week 26, subjects had bilateral hand radiographs and MRI of the hand with the greatest number of baseline tender and/or swollen joints.” The authors concluded: “Despite adequate blockade of IL-1, lutikizumab did not improve pain or imaging outcomes in erosive HOA [erosive hand osteoarthritis] compared with placebo.”

I said: I remain skeptic. I don’t see a niche for lutikizumab in the treatment of osteoarthritis. Bye bye!


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Thursday, January 17, 2019

Mavrilimumab discontinued



Adisinsight updated its information on Mavrilimumab on Dec. 12th 2018. I’ve just checked this source as I wanted to know more about the fate of Mavrilimumab after having listened to a talk by Prof. G.R. Burmester, one of the chief investigators on Mavrilimumab, last weekend.

Mavrilimumab is a human MAB for the treatment of rheumatoid arthritis. It targets the GMCSF [Granulocyte macrophage colony stimulating factor] receptor and alpha-chain. I’ve written about Mavrilimumab for the first time after the 2012 EULAR Meeting in Berlin.
I already harbored concerns about the drug: “Mavrilimumab did better than placebo, but the effect didn't last as long as the follow-up period after stopping the drug. The most common adverse events had been a decrease in CO diffusing capacity. Did any reader, who worked on studies, ever have to monitor CO diffusing capacity? As I haven't, this point leaves me a little bit uneasy.” Or: “My opinion: this doesn't seem to be the start of a success story. But still, as we need new drugs: All the best, Mavrilimumab!”

In January 2018 ME Weinblatt and colleagues published study details on: “A Randomized Phase IIb Study of Mavrilimumab and Golimumab in Rheumatoid Arthritis.” The authors concluded: “The findings of this study demonstrate the clinical efficacy of both treatments, mavrilimumab at a dosage of 100 mg every other week and golimumab at a dosage of 50 mg every 4 weeks, in patients with RA. Both regimens were well-tolerated in patients who had shown an inadequate response to DMARDs and/or other anti-TNF agents.”

In June 2017 GR Burmester and colleagues published study details on: “A randomised phase IIb study of mavrilimumab, a novel GM-CSF receptor alpha monoclonal antibody, in the treatment of rheumatoid arthritis.” The authors concluded: “Mavrilimumab significantly decreased RA disease activity, with clinically meaningful responses observed 1 week after treatment initiation, representing a novel mechanism of action with persuasive therapeutic potential.” Oh, with persuasive therapeutic potential! We’ll look into the persuasion quickly!

What is the news on this persuasive therapeutic potential? What does Adis Insight tell us? The indication of rheumatoid arthritis is discontinued. Adis Insight: “The US FDA places a clinical hold on a submitted IND application for a phase II trial in Giant cell arteritis, as additional information has been requested regarding the delivery device to be used in the trial”.

I’m still not convinced that Mavrilimumab could be a drug to treat inflammatory rheumatic diseases, though I am in favor for new ways of action as we already have enough TNF-alpha-inhibitors or IL-6-inhibitors. Maybe GMCSF [Granulocyte macrophage colony stimulating factor] simply isn’t a good target. Let’s hope that other targets work better.


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Saturday, May 5, 2018

The Mystery of Vobarilizumab (ALX-0061) 2nd Part


If you look for vobarilizumab at the ACR, the last publication has been at the 2014 meeting [1]. The conclusion had been: “ALX-0061 demonstrates in vitro a preferential binding profile for sIL-6R with a lesser activity for mIL-6R, while TCZ has a higher preference for mIL-6R. Preferential inhibition of sIL-6R trans-signalling by ALX-0061 could provide improved therapeutic efficacy with a better safety profile compared to TCZ.”

In 2016 AbbVie opted not to license vobarilizumab, but Ablynx wanted to seek a new partner for further development [2].

In March 2018 Ablynx announced that vobarilizumab did not meet the primary endpoint of dose response in a phase 2 study on systemic lupus erythematodes at week 24 [3]. IL-6 “induces terminal differentiation of B lymphocytes into antibody-forming cells and the differentiation of T cells into effector cells” [4] Pfizer discontinued a phase 2 study of PF-4236921 (an IL-6 inhibitor) for systemic lupus erythematosus in October 2015 [5]. But still stranger to me is the fact that tocilizumab hasn’t opted for an approval for lupus. As a matter of fact, if you search PubMed for tocilizumab in systemic lupus you’ll find about 20 studies, but none showing a move towards SLE as an indicated disease [6]. I once exploited the chance to talk to Professor Kishimoto (岸本忠三), who developed anti-IL-6 receptor therapy, but tocilizumab in SLE wasn't one of our topics. Still Ablynx tries to ride a dead horse.

I don’t see much room for vobarilizumab. I also don’t see any phase 3 study (RA) on the horizon. But let’s wait if motivation and conviction reappear as well as a sponsor for the needed phase 3 study shows up.


Links:
[1] Abstract Number: 1498; Maarten Van Roy and collaegues: ALX-0061, an Anti-IL-6R Nanobody® for use in Rheumatoid Arthritis, Demonstrates a Different in Vitro Profile As Compared to Tocilizumab - http://acrabstracts.org/abstract/alx-0061-an-anti-il-6r-nanobody-for-use-in-rheumatoid-arthritis-demonstrates-a-different-in-vitro-profile-as-compared-to-tocilizumab/
[6] Search in PubMed: "tocilizumab" [Supplementary Concept]) AND "Lupus Erythematosus, Systemic"[Mesh] https://www.ncbi.nlm.nih.gov/pubmed/?term=%22tocilizumab%22+[Supplementary+Concept]%29+AND+%22Lupus+Erythematosus%2C+Systemic%22[Mesh]


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Saturday, June 17, 2017

Sarilumab (ALX-0061) at the 2017 EULAR Annual Meeting in Madrid




My first encounter with sarilumab has been in 2011 at the ACR Annual Meeting in Chicago [1]. I had been quite disappointed at the 2012 ACR Annual Meeting in Washington [2]. At the 2015 ACR Annual Meeting in San Francisco sarilumab had been presented by several studies, but I still saw the need of data on radiographic progression [3].

There have been 10 studies on sarilumab presented at the 2017 EULAR Annual Meeting in Madrid.

M.C. Genovese and colleagues presented this study [4]: “ASSOCIATION BETWEEN CLINICAL AND RADIOGRAPHIC RESPONSES, AND PHYSICAL FUNCTION IN A PHASE 3 STUDY OF SARILUMAB PLUS METHOTREXATE IN PATIENTS WITH ACTIVE, MODERATE-TO-SEVERE RHEUMATOID ARTHRITIS”. Conclusions: “Achieving LDA [low disease activity] or remission, or absence of radiographic progression, was associated with overall greater improvement in physical function. Irrespective of whether patients achieved remission or LDA, SARILUMAB + MTX [methotrexate] showed greater improvements in HAQ-DI [health assessment questionnaire disability index] than Pbo [placebo] + MTX.”

G.R. Burmester and colleagues presented [5]: “EFFICACY AND SAFETY OF SARILUMAB MONOTHERAPY VERSUS ADALIMUMAB MONOTHERAPY IN PATIENTS WITH ACTIVE RHEUMATOID ARTHRITIS IN THE PHASE 3 MONARCH STUDY, INCLUDING SUBPOPULATIONS”. Conclusions: “SARILUMAB monotherapy demonstrated superiority to adalimumab monotherapy in the ITT [intention to treat] population in change from baseline in DAS28-ESR [disease activity score (for rheumatoid arthritis) on 28 joints, erythrocyte sedimentation rate]. The extent of treatment effect with SARILUMAB vs adalimumab was generally consistent across subpopulations. Overall incidences of AEs [adverse events] and serious AEs and rates of infection and serious infection were similar between groups”. This would have been expected as tocilizumab showed superiority versus adalimumab (C. Gabay and colleagues published [6]: “Tocilizumab monotherapy versus adalimumab monotherapy for treatment of rheumatoid arthritis (ADACTA): a randomised, double-blind, controlled phase 4 trial”.).

Sarilumab (Kevzara) received FDA approval on May 22, 2017. Sanofi and Regeneron Pharmaceuticals announced in April 2017, that the European Medicine Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion for the marketing authorization of Sarilumab (Kevzara).
Now, that the time is approaching for sarilumab to come to the market, I still ask myself: Do I need sarilumab? What could sarilumab give us, which we can’t get from tocilizumab? Will I split up my IL-6 inhibitor patients in two groups? Still I can’t answer these questions.


Links and References:
[4] Annals of the Rheumatic Diseases, volume 76, supplement 2, year 2017, page 576 / Session: Rheumatoid arthritis - other biologic treatment , (Poster Presentations) / DOI: 10.1136/annrheumdis-2017-eular.3513
[5] Annals of the Rheumatic Diseases, volume 76, supplement 2, year 2017, page 849 / Session: Rheumatoid arthritis - other biologic treatment , (Poster Presentations) / DOI: 10.1136/annrheumdis-2017-eular.4540

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