(The AACR-NCI-EORTC international conference was held Nov. 12-16 in San Francisco.)

Company (Location)

Product

Description

Indication

Status (Date)#


ACT Biotech Inc. (San Francisco)

Telatinib

An oral VEGF inhibitor

Gastric cancer

Phase II data showed patients treated with telatinib and Xeloda and cisplatin who responded with a large decrease of a specific angiogenesis biomarker were found to have a lower risk of disease progression and death compared with patients that had smaller decreases (11/15)

Cerulean Pharma Inc. (Cambridge, Mass.)

CRLX101

A camptothecin nanoparticle

Non-small-cell lung cancer

Phase I/IIa data showed that median progression-free survival time was 4.4 months for 21 of the 38 patients (11/15)

Enzon Pharmaceuticals Inc. (Piscataway, N.J.)

EZN-3042

An LNA oligonucloetide targeting survivn mRNA

Advanced solid malignancies

Phase I data demonstrated good tolerability and antitumor activity (11/15)

Exelixis Inc. (South San Francisco)

Cabozantinib

An inhibitor of MET, RET and VEGFR2

Metastatic castration-resistant prostate cancer

Phase I data suggested that a daily starting dose of 40 mg resulted in high rates of bone scan response assessed by computer-aided detection in men with CRPC and bone metastases; interim data on pain relief and related reduction in narcotic analgesic use showed 56% of patients decreased their dose by at least 30% (11/15)

Geron Corp. (Menlo Park, Calif.)

GRN1005

Lead LRP-directed peptide-paclitaxel conjugate

Brain metastases from solid tumors and malignant glioma

Phase I data demonstrated single-agent clinical activity in both indications (11/16)

MethylGene Inc. (Montreal)

MGCD265

Oral Met/VEGF receptor tyrosine kinase inhibitor

Advanced solid cancers

Phase I data showed the compound was tolerable, with no treatment-related serious adverse events, and showed early signs of clinical benefit (11/15)

Myrexis Inc. (Salt Lake City)

MPC-3100

Heat-shock protein inhibitor

Cancer

Phase I data showed that it was generally safe and well tolerated (11/15)

Oncolytics Biotech Inc. (Calgary)

Reolysin

Intravenous therapy

Advanced pancreatic cancer

Interim Phase II data of Reolysin in combination with gemcitabine showed that all but one of 12 patients reported symptomatic improvement, including seven with stable disease for 12 weeks or longer, for a clinical benefit rate of 58% (11/15)

Oncothyreon Inc. (Seattle)

PX-866

Irreversible, pan-isoform phosphatidylinositol-3-kinase inhibitor

Advanced cancer

Two Phase I/II trials showed no dose-limiting toxicities with the combination of docetaxel and PX-866 generally well tolerated; best response was stable disease in 21 of 28 patients and progressive disease in seven patients, for a disease control rate of 75% (11/15)

Pieris AG (Freising-Weihenstephan, Germany)

PRS-050

Anticalin; an anti-VEGF targeted protein therapeutic

Advanced solid tumors

Phase I data showed it was well tolerated, with no maximum-tolerated dose reached, and it demonstrated biological activity, with no immunogenicity (11/16)

Syndax Pharmaceuticals Inc. (San Francisco and Waltham, Mass.)

Exemestane

Hormone therapy

Postmenopausal estrogen-receptor positive breast cancer

A pharmacodynamic analysis in a subset of patients demonstrated an association of the pharmacodynamic marker lysine hyperacetylation with clinical outcome (11/15)

TetraLogic Pharmaceuticals (Malvern, Pa.)

TL32711

Smac mimetic candidate

Solid tumors and lymphomas

Phase I data suggested it caused potent and sustained suppression of inhibitor of apoptosis protein in patient peripheral blood mononuclear cells and tumor biopsies over seven days at tolerable dose levels (11/15)

Ziopharm Oncology Inc. (New York)

Zymafox

Palifosfamide

Non-small-cell lung cancer

Phase Ib data showed that Zymafos in combination with etoposide and carboplatin can be given at a maximum-tolerated dose of 130 mg/m2, with a dose-limiting toxicity of neutropenic fever (11/15)


Notes:

Public biotech company stock symbols can be found in the stock report located on the last two pages of this issue.

# The date indicated refers to the BioWorld Today issue in which the news item can be found.