
Stemcentrx
Develops innovative therapies for cancer.
Date | Investors | Amount | Round |
---|---|---|---|
$23.5m | Late VC | ||
$42.0m | Series D | ||
$200m | Series F | ||
$250m | Series G | ||
$10.2b Valuation: $10.2b | Acquisition | ||
Total Funding | $515m |







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Stemcentrx was a biotechnology firm established in 2008 with a specific mission: to develop therapies targeting cancer stem cells (CSCs), which are believed to initiate and perpetuate tumors. The company was co-founded by Brian Slingerland, who served as CEO, and Scott Dylla, who was the Chief Scientific Officer. Slingerland brought a strong financial background to the venture, having previously been a managing director at Goldman Sachs and a co-founder of the investment bank Qatalyst Partners. His motivation was deeply personal, driven by the loss of three relatives to cancer. Dylla provided the scientific leadership, drawing on his experience as a senior scientist at OncoMed Pharmaceuticals and a postdoctoral scholar at Stanford University, where he focused on stem cell biology and cancer.
The company's core business model was centered on the discovery and development of novel cancer drugs. Stemcentrx built an integrated platform that encompassed target discovery, in-house GMP manufacturing, and clinical development capabilities, allowing it to move from the lab to clinical trials efficiently. Its primary focus was on creating antibody-drug conjugates (ADCs), a class of drugs designed to deliver a potent toxin directly to cancer cells while sparing healthy tissue. The business strategy involved identifying novel targets on the surface of cancer stem cells and then engineering ADCs to attack those specific targets. This approach led to partnerships with major pharmaceutical companies like Pfizer and Bristol Myers Squibb.
The company's most prominent product candidate was Rovalpituzumab tesirine, or Rova-T. This ADC was engineered to target delta-like protein 3 (DLL3), a protein highly expressed in tumors associated with small-cell lung cancer (SCLC) but minimally present in normal tissues. By 2015, Stemcentrx emerged from stealth mode with an impressive pipeline of five drugs in human clinical trials for various cancers, including SCLC, ovarian, and triple-negative breast cancer. The promising early data for Rova-T, showing significant response rates in pre-treated SCLC patients, generated considerable excitement.
This early success and the perceived potential of its ADC platform culminated in a landmark event in 2016 when AbbVie acquired Stemcentrx. The deal was valued at approximately $5.8 billion in cash and stock, with an additional $4 billion in potential milestone payments, making it one of the largest private biotech acquisitions at the time. However, the promise of Rova-T did not materialize in later-stage clinical trials. Subsequent studies, including the Phase II TRINITY and Phase III TAHOE trials, showed disappointing results, with modest efficacy and, in some cases, inferior outcomes compared to standard chemotherapy. Ultimately, AbbVie halted the entire Rova-T research and development program and wrote off a significant portion of its investment in Stemcentrx.
Keywords: Stemcentrx, Scott Dylla, Brian Slingerland, antibody-drug conjugate, ADC, cancer stem cells, Rovalpituzumab tesirine, Rova-T, small-cell lung cancer, SCLC, DLL3 target, oncology therapeutics, AbbVie acquisition, GMP manufacturing, clinical trials, cancer research, solid tumors, biomarker-specific therapy, biotechnology, target discovery