CHROMA announces Positive Phase II Efficacy Data for Novel Cancer Therapy Tosedostat - Gilde Healthcare

CHROMA announces Positive Phase II Efficacy Data for Novel Cancer Therapy Tosedostat

December 11, 2008

Oxford – Chroma Therapeutics Limited, a leading European specialist cancer research company, announced today positive data from a Phase II study with its oral, once-daily experimental cancer therapy tosedostat (CHR-2797) in the treatment of patients with acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) who have failed on, or who are unsuitable for, chemotherapy.

Headline data from the study, which was presented at the December 2008 American Society of Hematology (ASH) meeting, were as follows:

  • 10 out of 38 AML patients (26%) treated showed a complete or partial response to therapy during the study;
  • of three MDS patients treated in this study, one showed a partial response and one achieved stable disease;
  • despite a poor prognosis upon entering the study, 10 out of 41 patients were able to continue treatment beyond the 84 days specified in the protocol; and
  • the drug was very well-tolerated during the study

Chroma is currently preparing for a registration study with tosedostat in AML, to commence during 2009.

Ian Nicholson, Chief Executive Officer of Chroma, commented: “We are very pleased that this Phase II study, in patients with a poor prognosis, has confirmed the activity we saw in earlier studies. We look forward to accelerating tosedostat into Phase III registration studies during 2009, particularly in light of the lack of treatment options currently available for patients with this debilitating disease”.

The full abstract presented at the ASH meeting is available at the company’s website, www.chromatherapeutics.com.

About aminopeptidases and tosedostat (CHR-2797)

Aminopeptidases are a family of intracellular enzymes involved in the supply of amino acids that are essential for cell growth. Inhibition of aminopeptidases has been shown to halt cell growth or cause apoptosis (cell death) in a large number of cancer cell lines. Conversely, normal (non-tumour) cell lines have been shown to be insensitive to aminopeptidase inhibition. Tosedostat is a potent inhibitor of aminopeptidases that has demonstrated strong preclinical efficacy as monotherapy and has also been shown to strongly synergise with a number of leading cancer therapies in a range of cancer cells.

About Chroma Therapeutics

Chroma Therapeutics, based in Oxford (UK), is a drug discovery and development company focused in the fields of oncology and inflammatory disorders. Chroma is building a broad pipeline of first- or best-in-class treatments utilising its expertise in chromatin biology and its novel intracellular accumulation technologies, which include the ability to selectively target drugs to macrophages. Chroma is backed by a number of leading specialist investors, including Abingworth, Essex Woodlands, Gilde Healthcare Partners, Nomura Phase4 and The Wellcome Trust.

More information about Chroma can be found at www.chromatherapeutics.com

Gilde Healthcare participates in $150M Series D financing of CatalYm

Proceeds will expand late-stage clinical development of lead programme visugromab’s into earlier lines of treatment including checkpoint naïve and second-line settings in randomized, controlled studies in select solid tumor indications Round brings on board new international...
July 16, 2024

Gilde Healthcare portfolio company Eetgemak joins forces with TotaalVERS to become the leading integrated healthcare foodservice provider

Combining TotaalVERS and Eetgemak will form a leading end-to-end foodservice provider*, offering a wide range of convenience meals, ingredients and groceries to the healthcare sector. The partnership emphasizes commitment to quality, service, and innovation in...
July 5, 2024

Gilde Healthcare company Volta Medical announces positive results from transatlantic trial on AI-assisted ablation for persistent atrial fibrillation

TAILORED-AF randomized controlled trial (RCT) findings demonstrated superiority in freedom from atrial fibrillation (AF) at 12 months from a tailored cardiac ablation guided by artificial intelligence (AI) when compared to pulmonary vein isolation (PVI) alone....
May 21, 2024