Advertisement
Canada markets open in 28 minutes
  • S&P/TSX

    21,871.96
    +64.59 (+0.30%)
     
  • S&P 500

    5,010.60
    +43.37 (+0.87%)
     
  • DOW

    38,239.98
    +253.58 (+0.67%)
     
  • CAD/USD

    0.7302
    +0.0001 (+0.01%)
     
  • CRUDE OIL

    80.94
    -0.96 (-1.17%)
     
  • Bitcoin CAD

    90,610.28
    +132.33 (+0.15%)
     
  • CMC Crypto 200

    1,418.72
    +3.96 (+0.28%)
     
  • GOLD FUTURES

    2,324.30
    -22.10 (-0.94%)
     
  • RUSSELL 2000

    1,967.47
    +19.82 (+1.02%)
     
  • 10-Yr Bond

    4.6460
    +0.0230 (+0.50%)
     
  • NASDAQ futures

    17,416.25
    +66.25 (+0.38%)
     
  • VOLATILITY

    16.55
    -0.39 (-2.30%)
     
  • FTSE

    8,035.24
    +11.37 (+0.14%)
     
  • NIKKEI 225

    37,552.16
    +113.55 (+0.30%)
     
  • CAD/EUR

    0.6840
    -0.0010 (-0.15%)
     

Roche gene testing key to $1.7 billion deal for Blueprint cancer drug

FILE PHOTO: Logo of Swiss drugmaker Roche at its Basel headquarters

By John Miller

ZURICH (Reuters) - Roche has struck a $1.7 billion cancer drug pact with Blueprint Medicines, it said on Tuesday, as advances in genetic testing for rare mutations drive lucrative deals for expensive treatments.

The Swiss drugmaker will pay $675 million in cash and make a $100 million equity investment in Blueprint for rights to pralsetinib, which could gain U.S. approval against so-called RET-altered non-small cell lung cancer in November.

U.S. company Blueprint, which has been working with Roche since 2016, could also receive up to $927 million in milestone payments, plus royalties on sales outside the United States, Roche said in a statement.

ADVERTISEMENT

Mutations to the RET gene can drive tumour growth, but given that such genetic changes occur in only a fraction of patients with lung or thyroid cancer, genetic testing is key to prescribing the most beneficial drugs.

Roche's diagnostics division is key to a deal that will enable the company to expand on a portfolio of medicines such as Alecensa and Rozlytrek, which require testing to determine which patients will benefit.

"We will leverage our global reach and expertise in oncology, as well as our capabilities in diagnostics," said James Sabry, Roche's head of partnerships.

Beyond lung cancer, Blueprint has also submitted pralsetinib to the U.S. Food and Drug Administration (FDA) for treating advanced RET mutant and RET fusion-positive thyroid cancers.

Roche and Blueprint are not alone in combining sophisticated diagnostics with niche drugs.

Eli Lilly and Co and German drugmaker Bayer's Vitrakvi also targets tumours with a rare mutations identified by testing. Novartis and Incyte, meanwhile, won approval this year for lung cancer drug Tabrecta, which also requires genetic testing.

Both Tabrecta and Vitrakvi rely on a diagnostic test from Roche's Foundation Medicine diagnostics unit.

Though such gene mutations affect relatively few patients, the companies aim to turn their medicines into blockbusters by commanding prices running into the tens of thousands of dollars per month.

Tabrecta costs $18,000 a month, Roche's Rozlytrek is priced similarly and Vitrakvi lists at $32,800 a month.

(Reporting by John Miller; Editing by Brenna Hughes Neghaiwi and David Goodman)