Skip to content

Posts tagged ‘XL184’

MDV3100 in Advanced Prostate Cancer

November 9th, 2011

Daedalus

The fast moving prostate cancer market took another leap forward last week with the announcement of positive phase III data for Medivation’s MDV3100.

As reported by Sally Church on Pharma Strategy Blog, Medivation announced that the interim analysis of the AFFIRM trial showed a 4.8 month increase in overall survival (OS) compared to placebo.

Although this is only interim and not final data, Sally observed:

“the 4.8 month improvement in OS in post-chemo setting is superior to that previously seen reported for abiraterone (Zytiga), which had a 3.9 month advantage over placebo.”

Pieter Droppert on Biotech Strategy Blog noted, MDV3100 and Zytiga have completely different mechanisms of action in advanced prostate cancer.

MDV3100 is an androgen receptor blocker, while Zytiga is an androgen biosynthesis inhibitor. This distinction is key.  Zytiga inhibits the CYP17 enzyzme complex required for androgen biosynthesis. However, a consequence of CYP17 inhibition is an increase in mineralocorticoid levels, which can lead to hypokalemia, hypertension, fluid retention.

The result is that Zytiga requires coadministration of a corticosteroid (prednisone) to reduce the incidence and severity of potential mineralocorticoid adverse reactions.

MDV3100 does not require the administration of a steroid, which is a big advantage to patients.  Instead it blocks the androgen receptor (AR) that is highly expressed on prostate cancer cells.

EMCC 2011 Sternberg Challenges to Developing New Advanced Prostate Cancer Drugs 1024x768 MDV3100 in Advanced Prostate CancerCora Sternberg presents Prostate Cancer Educational Symposia at EMCC 2011 in Stockholm

There are a lot of new products in the pipeline for prostate cancer including TAK-700, Cabozantinib (XL184), radium-223 chloride (Alpharadin), BPX-101, Prostvac-VF, ipilumumab, Custirsen (OGX-011), dasatinib (Sprycel), lenalidomide (Revlimid) and ARN-509 to name a few.

The prostate cancer market is forecast to grow from $1B to $5B by 2015 as new products are approved and new treatment options become available. This is good news for advanced prostate cancer patients.

Why is cabozantinib (XL184) so interesting in cancer?

October 25th, 2011

Daedalus

As reported by Sally Church, PhD on Pharma Strategy Blog yesterday, Exelixis announced positive phase 3 trial data for cabozantinib in medullary thyroid cancer (MTC).

There are four main types of thyroid cancer:

  • papillary
  • follicular
  • medullary
  • anaplastic.

According to the NCI there are 48,000 new thyroid cancer cases a year in the United States and 1700 deaths.  Medullary thyroid cancer is estimated to be only 5-8% of cases, and thyroidectomy is curative in a high percentage of cases.  This low incidence, therefore, makes this a small target market.

As noted on Pharma Strategy Blog, the topline data for cabozantinib in MTC showed an increase in progression free survival  (PFS) of 7.2 months.

This is good news for MTC patients. Earlier this year AstraZeneca’s vandentanib (Caprelsa®) was approved by the FDA in medullary thyroid cancer, but as Pharma Strategy Blog mentioned, it has a number of challenges:

“namely prolongation of QT, causing irregular heart beat and thus it was made available under a Risk Evaluation and Mitigation Strategy (REMS).”

Cabozantinib XL184 Exelixis banner Why is cabozantinib (XL184) so interesting in cancer?What makes cabozantinib (XL184) so interesting in cancer drug development?

As Sally noted in her insightful blog post, cabozantinib “targets MET, RET and VEGFR2.

It is a targeted therapy that inhibits both MET and VEGFR.  MET and its ligand HGF drive tumor cell invasion and metastasis.  MET and VEGFR2 synergize to promote angiogenesis.

In approximately half of the patients with sporadic MTC, there are germline mutations of RET (Rearranged during Transfection) gene. MTC mutations activate the RET kinase, and several signaling pathways including the RAS/MEK/ERK/PI3K pathway. This in turn promotes cell proliferation, invasion and survival.

At the annual meeting of the American Society of Clinical Oncology (ASCO) in Chicago earlier this year, phase 2 data for cabozantinib in metastatic castration resistant prostate cancer was presented. The preliminary results showed a dramatic effect on bone pain and narcotic use. Validation of these results that may have a big impact on the quality of life for advanced prostate cancer patients is awaited in a more formal pain study.

Cabozantinib is an interesting broad-acting product to watch out for and further data in ovarian and prostate cancer is expected. You can follow its development on Pharma Strategy Blog.

ASCO 2011 Olaparib and Cabozantinib are two new products to watch

May 24th, 2011

Daedalus

The countdown is underway for the 2011 annual meeting of the American Society of Clinical Oncology (ASCO) in Chicago from June 3-7th.  Over 30,000 attendees are expected and more than 4,000 abstracts will be presented.

What’s hot at the meeting is what everyone is asking?  Sally Church is preparing a video blog (vlog) with her thoughts that will be posted on Pharma Strategy Blog soon.

In the meantime, two new products to watch out for are:

Cabozantinib (XL184).  This new product from Exelixis may have potential in advanced prostate cancer with phase II data showing a dramatic effect on bone metastases, making it a potential competitor to denosumab.  You can read more about the ASCO data on Biotech Strategy Blog.

Olaparib.  Just when we thought that PARP inhibitors were ineffective after the failure of iniparib in breast cancer, there’s dramatic data at ASCO showing AstraZeneca’s olaparib prolongs remission in serious ovarian cancer.  You can read more on Pharma Strategy Blog.

The focus of ASCO 2011 is “Patients, Pathways, Progress”. We’ll be writing more about the meeting over the next few weeks, so do check back for more details.