Clinical Trial Success Rates Still Dismal, But Certain Sectors Outperform

The high risk-high reward nature of drug development is a constant challenge to pharma. Informa's Pharma Intelligence teamed up with BIO and Amplion to provide an update on clinical development success rates from 2006 to 2015, including a new analysis on trials incorporating patient selection biomarkers.

High-profile failures in the drug industry can break a company. In immuno-oncology, one of the hottest areas in drug development, Aduro Biotech Inc. – a fairly young firm, founded in 2008 through the merger of Triton and Oncologic [See Deal] – had high hopes for GVAX Pancreas, a whole tumor cell vaccine that secretes granulocyte-macrophage colony stimulating factor in an effort to prompt the immune system's attack on the cancer. (Aduro licensed GVAX from BioSante [now part of ANI Pharmaceuticals Inc.] in 2011 [See Deal].) The candidate advanced to Phase IIb and was being tested in combination with CRS207 (a proprietary attenuated strain of Listeria that expresses human mesothelin, also from Aduro) in the ECLIPSE trial, but failed to meet its overall survival endpoint in the third-line setting for pancreatic cancer, actually posting a shorter median overall survival time compared with CRS207 alone or chemotherapy. Aduro's shares took a hit, dropping 20% at closing on the day of the announcement in May 2016. The company is still going to be evaluating a triple combination of GVAX, CRS207 and Bristol-Myers Squibb Co.'s Opdivo (nivolumab) in the ongoing STELLAR trial. Aduro has other GVAX vaccines in the pipeline, too, but the pancreatic cancer candidate is its lead, and potentially is closest to market. Likewise, Celldex Therapeutics Inc.'s Rintega (rindopepimut) vaccine was another high-profile casualty. In March 2016, an independent data safety and monitoring board (DSMB) stated that Rintega would not reach statistical significance for overall survival in patients with newly diagnosed EGFRvIII-positive glioblastoma with minimal residual disease in the Phase III ACT IV study. The DSMB determined that, following an interim analysis, the control arm of generic temozolomide outperformed Rintega, and Celldex terminated the study. (See[A#14160307003].) The news sent Celldex's stock value into a tailspin, dropping more than 50% after the DSMB's determination, and the share price hasn't recovered since.

[Sidebar#2016800109]

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on In Vivo for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Market Intelligence

PBMs Tighten The Reins: Value Becomes The New Access Gatekeeper

 
• By 

Facing rising costs and tighter regulations, PBMs and insurers are accelerating the shift to value-based drug coverage, demanding stronger proof of therapeutic and economic benefit from pharma.

Financing Quarterly Statistics, Q2 2025

 
• By 

During Q2, biopharmas brought in an aggregate $17.5bn in financing and device company fundraising totaled $2.7bn; while in vitro diagnostic firms and research tools players raised $1.7bn

When VC Steps Back: Finding Alternative Biotech Funding

 
• By 

The biotech funding landscape is undergoing a fundamental shift. With traditional VC becoming increasingly cautious and selective, industry executives are exploring new avenues for capital. Conversely, this evolution may ultimately benefit the sector's long-term sustainability.

Navigating the GLP-1 Opportunity In China: Strategic Imperatives For Western Pharma

 
• By 

The Chinese appetite for GLP-1s is noticeable. While the market opportunity for western pharma is huge, so are the strategic market access challenges, though not unsurmountable, L.E.K. Consulting told In Vivo.

More from In Vivo

Future Proofing Gene Therapy Assays For Regulatory Success

 
• By 

As gene therapy advances and regulations tighten, biopharma companies face growing pressure to design diagnostic assays that are both flexible and future ready. Strategic early investment in assay development can prevent costly delays and rework as therapies progress toward approval.

Podcast: Poolbeg CEO On The Biotech’s Big Bet On Small Molecules

 
• By 

In the latest episode of the In Vivo Podcast, Jeremy Skillington, CEO of Poolbeg Pharma, discussed the company’s ambitious pipeline and strategic direction.

video
Sponsored by:

Meeting the demands of the global biologics market

Lonza is addressing the growing global demand for biologics by utilizing its expert teams and the advanced capabilities of its newly acquired large-scale manufacturing site in Vacaville, California. Joanna McCafferty, Director of Commercial Development, shares more in this brief video. Ask ChatG