CBMG shows strong data in early CART trials

Chinese biotech Cellular Biomedicine Group (CBMG) shed some light on its early stage cancer immunotherapy program during an investor day in New York on 25 March. The company presented data from Phase I trials in a small number of patients that were treated with their chimeric antigen receptor-T cell (CART) technology. The CART space has been one of the hottest areas in oncology over the last year as big players like Novartis and smaller players like Cellectis have moved their therapies forward and shown impressive results in clinical trials; most recently, Cellectis increased the amount it plans to raise in an IPO by 70% to $197m based on the strength of its CART programs. CBMG is hoping to join the frenzy. The Chinese biotech reported that nine patients with relapsed or chemo-refractory B-cell acute lymphocytic leukemia received its CAR-CD19 T-cell therapy. Two of nine patients, or 22.2%, showed a complete response, while four of nine patients, or 44.4%, achieved a partial response – resulting in a 66.7% overall response rate (ORR). Meanwhile, seven patients with advanced diffuse large B-cell lymphoma were given the company's CAR-CD20 T-cell therapy. One of the two patients in the trial with no bulky tumors achieved a 14-month durable and ongoing complete remission and another achieved a 6-month tumor regression resulting in an ORR of 100%. Three of four patients with evaluable bulky tumor burden achieved three to six month tumor regression for an ORR 75%. While the results are encouraging, the data is very early and the number of patients in the trial is too small to be translatable to later-stages.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip 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 Anticancer

Merus Bispecific Impresses In Head And Neck Cancer

 

Updated Phase II results from petosemtamab have impressed ahead of ASCO, outshining Keytruda monotherapy and its bispecific rival from Bicara.

Boehringer’s CMO On How AI, Integrated Evidence Generation Underpin Its Ambitious Launch Plans

 

The German company has big plans for the next five years or so. Scrip speaks to its chief medical officer Lykke Hinsch Gylvin about how it is using AI and other innovative approaches to make good on its ambitions.

End Is Nigh For 4SC After EMA’s No For Kinselby

 
• By 

The German biotech has discontinued the oral HDAC inhibitor for cutaneous T-cell lymphoma.

Japan Pharma Sees US Revenues Grow But Policy Impact Still Unclear

 
• By 

Japanese majors put in generally solid performances in the fiscal year ended 31 March, but overseas revenues and forex effects, rather than the domestic market, provided most of the growth.

More from Therapy Areas

New Vaccine Framework Avoided Worst-Case Scenario, Analysts Say

 
• By 

The new US FDA vaccine guidelines introduced on 20 May might cause financial woes for Moderna, but overall vaccine makers should not be as impacted as feared.

Merck KGaA Plans Phase III For Enpatoran After Mixed Phase II Lupus Data

 

The Phase II study testing the novel TLR7/8 inhibitor met the primary endpoint in a cohort of patients with cutaneous lupus erythematosus and systemic lupus erythematosus with rash, but did not in patients with SLE.

PureTech’s IPF Candidate Ready For Phase III After Efficacy Win

 

Coming one day after Boehringer’s underwhelming data, PureTech’s tweaked molecule, deupirfenidone, shows promise in slowing idiopathic pulmonary fibrosis.