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

Will AstraZeneca Reach Summit And Be A PD-1xVEGF Player?

 
• By 

Rumor mill suggests a $15bn licensing deal for ivonescimab is in the offing.

Dizal’s Zegfrovy Wins US NSCLC Approval, At Lower Dose Than In China

 

Dizal's EGFR inhibitor Zegfrovy approved in US as new once-daily oral option for second-line NSCLC with EGFR exon 20 insertion mutations, at lower dose than in China.

Regeneron Wins Long-Sought FDA Nod For Lynozyfic In Myeloma

 

The agency gave accelerated approval to the BCMAxCD3-directed bispecific antibody, which had been the subject of an August 2024 CRL.

BerGenBio Plumps For Oncoinvent From Long List Of 50 Suitors

 
• By 

The merger with a fellow Norwegian biotech comes a few months after its lead asset, bemcentinib, bit the dust.

More from Therapy Areas

Novartis’s Cosentyx Suffers Rare Phase III Fail

 
• By 

Multi-blockbuster falls short in a giant cell arteritis study.

In Brief: 4DMT Fast-Tracks Long-Acting Wet AMD Therapy Trials, Cuts 25% Of Workforce

 

4D Molecular Therapeutics has fast-tracked its Phase III trials for 4D-150 in wet AMD, with top-line data from one now expected in H1 2027 and another underway ahead of schedule. The company is also cutting a quarter of its staff as it focuses on its late-stage pipeline and to help fund the trials.

Regeneron Wins Long-Sought FDA Nod For Lynozyfic In Myeloma

 

The agency gave accelerated approval to the BCMAxCD3-directed bispecific antibody, which had been the subject of an August 2024 CRL.