Innovation and Progress
1992-1999: Discovery & Development
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1992 |
Invention of CID by David Spencer and Gerald Crabtree (Stanford), and Stuart Schreiber (Harvard); published in Science |
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1994 |
Stanford licenses CID intellectual property to ARIAD Gene therapeutics, Inc |
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1995 |
First demonstration of CID-regulated iFAS suicide switch, and first demonstration of use in vivo in transgenic mice |
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1996 |
ARIAD designs fully synthetic, high specificity dimerizers, including AP1903 (for clinical use) and AP20187 (ARGENT® technology, for research use, later licensed to >1,000 research groups worldwide) |
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1998 |
The year of iCaspase: papers published by four independent research groups (Spencer, Dixit, Baltimore and Lenardo) |
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1999 |
First iCaspase9 paper published (precursor to CaspaCIDe™) |
2000-2010: Clinical Applications
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2000 |
ARIAD sponsors AP1903 phase I clinical trial |
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2003 |
Invention of inducible CD40 (iCD40) (precursor to DeCIDe™) by David Spencer, Kevin Slawin and colleagues (Baylor College of Medicine) |
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2004 |
Bellicum founded based on iCD40 intellectual property |
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2005 |
First demonstration that iCaspase9 can be used to efficiently eliminate primary T cells in vivo with little (if any) effect on T cell function |
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2006 |
Bellicum and ARIAD execute first clinical license for CID intellectual property |
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2006 |
First closing of angel financing |
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2007 |
Invention of inducible MyD88 (iTLR) costimulatory molecule by David Spencer and colleagues, subsequently licensed by Baylor to Bellicum |
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2007 |
Bellicum receives $1.45 million award from Texas Emerging Technology Fund
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2008 |
BPX-101 IND allowed by FDA |
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2009 |
Series A financing completed |
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2009 |
Initiation of Phase I/II clinical trial (BP-PC-001) of BPX-101 + AP1903 |
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2009 |
Initiation of Phase I clinical trial (CASPALLO) of iCaspase9 by Malcolm Brenner (Baylor Center for Cell & Gene Therapy) |
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2010 |
Interim results of BP-PC-001 trial presented at AACR |
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2010 |
Interim results of CASPALLO trial presented at ASGT
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2010 |
Demonstration of iCaspase9 functionality in mesenchymal stem cells |
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