Advertisement covers ICAAC 2014


BMS-986001 Bone, Metabolic Data Compare Well to Tenofovir Through 48 Weeks

October 10, 2014

 1  |  2  |  Next > 

There's more than one nucleoside analog reverse transcriptase inhibitor (NRTI) working its way through the antiretroviral pipeline. Although most eyes have been focused on the progress of tenofovir alafenamide fumarate (TAF), the patient-friendlier prodrug of tenofovir (Viread), another thymidine analog is moving through development as well: BMS-986001.

Actually, the name of the drug is now technically OBP-601: It was initially being codeveloped by Oncolys BioPharma and Bristol-Myers Squibb (BMS), but BMS terminated the development agreement. It is up to Oncolys, a small biopharmaceutical company, to further develop the drug on its own or seek a new partnership.

While OBP-601's future remains in flux, data continue to flow forth from its previous incarnation as BMS-986001. ICAAC 2014 featured a pair of presentations exploring the safety and efficacy of the drug at 48 weeks in antiretroviral-naive patients. The overarching efficacy and safety data were presented in an oral abstract session by Samir K. Gupta, M.D., M.S., while a closer examination of bone and metabolic impact was presented in a poster by Grace McComsey, M.D., a professor of pediatrics and medicine at the Case Western Reserve University School of Medicine in Cleveland.

I spoke with McComsey at her poster to discuss the study results and other questions surrounding the development of BMS-986001/OBP-601.

What is BMS-986001?

That's a new NRTI that's a thymidine analogue. This [poster] is looking at the safety data. The reason is: Obviously, the thymidine analogues d4T and AZT had very bad metabolic data, which caused people not to use them. This [aims to be part of] the better, new generation of thymidine analogues. This poster is looking at safety data from bone, to lipids, to fat tissue -- both peripheral and visceral fat. In terms of bone: First, comparing three different doses of this NRTI, compared to tenofovir, I think the results were expected. Tenofovir, like with any other study, led to greater drop in hip BMD, as well as lumbar spine BMD, compared to the NRTI that we're testing [BMS-986001].

Like I said, this is not unusual; this is comparable to the data with TAF, compared to tenofovir.

You see some decrease in BMD, like you see with any other regimen, but it's not to the same extent that we're seeing with tenofovir.

Is this a reflection of the effect all antiretrovirals have on bone density, or is this just age-related bone decline that we're seeing?

We know, actually, [with] every antiretroviral regimen tested to date: When you first start it, the first 24 to 96 weeks, you'll see a decrease in BMD. Usually it's between 2% and 6%. Then it stabilizes after that. It doesn't recover; that's the bad thing. It stabilizes; it doesn't get back to normal. It's more accentuated than just age -- just spending a year of life. That's not going to drop the BMD that much. Mainly, most of these people are men, median age [between] 31 and 32. So you don't expect them to lose any significant bone mass during that time.

I know we've had studies suggest that reduction of BMD doesn't necessarily result in actual fracture risk increasing, or any kind of real demonstrable clinical impact.

Right. But actually there are a lot of other data -- including some cohorts -- showing that BMD, even in HIV patients, does relate to fractures. So people who had low BMD by DEXA ended up having fractures.

I think the reason the data is conflicted [is] because we don't have enough long-term follow-up yet. We're just starting to learn about bone. The first bone studies we did were probably in 2004 or 2005. That's nothing. Five years or 10 years of bone data is nothing. You need decades.

All right. Let's talk fat AND BMS-986001.

When you talk fat you always worry about two things: lipoatrophy, which is limb fat loss, as well as accumulation of fat.

So we looked at, by DEXA scan, limb fat versus trunk fat. And we looked by CT scan -- CT is better because it shows you visceral fat as well as subcutaneous fat. The data was consistent with both methods: We didn't see loss of fat. What we saw is gain of fat.

And the gain, with all the different arms, [was] mainly with the highest dose of 400 QD [of BMS-986001]: [It] seemed to be worse than tenofovir.

To what extent is this a reflection of people recovering fat from baseline, as opposed to actually having a fat problem?

Right. That's what I was telling people. Everybody's asking me, "Is this bad?" We don't know. What we know is ACTG-5224, which I had chaired, found exactly the same data when abacavir [Ziagen] was compared to tenofovir. We also saw that abacavir had more gain of fat compared to tenofovir.

So you can say maybe tenofovir somehow interferes with the normal return to health. Or maybe it's a pathological increase of fat. Nobody knows yet.

 1  |  2  |  Next > 

This article was provided by TheBodyPRO. It is a part of the publication The 54th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC 2014).

No comments have been made.

Add Your Comment:
(Please note: Your name and comment will be public, and may even show up in
Internet search results. Be careful when providing personal information! Before
adding your comment, please read's Comment Policy.)

Your Name:

Your Location:

(ex: San Francisco, CA)

Your Comment:

Characters remaining:

Please note: Knowledge about HIV changes rapidly. Note the date of this summary's publication, and before treating patients or employing any therapies described in these materials, verify all information independently. If you are a patient, please consult a doctor or other medical professional before acting on any of the information presented in this summary. For a complete listing of our most recent conference coverage, click here.


The content on this page is free of advertiser influence and was produced by our editorial team. See our content and advertising policies.