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DRUG:

L-DOS47

i
Other names: L-DOS47, L-DOS 47, L-DOS-47
Associations
Trials
Company:
Helix BioPharma
Drug class:
CEACAM6 inhibitor, Urease stimulant
Associations
Trials
18d
L-DOS47 Plus Doxorubicin in Advanced Pancreatic Cancer (clinicaltrials.gov)
P1/2, N=28, Active, not recruiting, Helix BioPharma Corporation | Recruiting --> Active, not recruiting | N=20 --> 28 | Trial completion date: Aug 2025 --> Nov 2024
Enrollment closed • Enrollment change • Trial completion date • Metastases
|
doxorubicin hydrochloride • L-DOS47
6ms
A Dose Escalation Study of L-DOS47 in Recurrent or Metastatic Non-Squamous NSCLC (clinicaltrials.gov)
P1, N=14, Terminated, Helix BioPharma Corporation | Completed --> Terminated; Slow enrolment - standard of care evolved over the duration of the study such that treatment regimen employed in the study was no longer current standard of care for first line resulting in recruitment challenges.
Trial termination • Combination therapy • Metastases
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
carboplatin • pemetrexed • L-DOS47
9ms
L-DOS47 Elevates Pancreatic Cancer Tumor pH and Enhances Response to Immunotherapy. (PubMed, Biomedicines)
Using chemical exchange saturation transfer-magnetic resonance imaging (CEST-MRI) to measure the tumor extracellular pH (pHe), we confirmed that L-DOS47 raises the tumor pHe from 4 h to 96 h post injection in acidic tumors (average increase of 0.13 units). Additional studies showed that combining L-DOS47 with anti-PD1 significantly increases the efficacy of the anti-PD1 monotherapy, reducing tumor growth for up to 4 weeks.
Journal
|
CEACAM6 (CEA Cell Adhesion Molecule 6)
|
L-DOS47
1year
L-DOS47 Plus Doxorubicin in Advanced Pancreatic Cancer (clinicaltrials.gov)
P1/2, N=20, Recruiting, Helix BioPharma Corporation | Trial completion date: Aug 2023 --> Aug 2025 | Trial primary completion date: Aug 2023 --> Aug 2024
Trial completion date • Trial primary completion date • Metastases
|
doxorubicin hydrochloride • L-DOS47
2years
A Phase 1, Open-Label, Dose-Escalation Study of L-DOS47 in Combination With Pemetrexed Plus Carboplatin in Patients With Stage IV Recurrent or Metastatic Nonsquamous NSCLC. (PubMed, JTO Clin Res Rep)
There was an apparent association between best overall response rate and highest anti-L-DOS47 antibody titer measured. L-DOS47 combined with standard pemetrexed and carboplatin chemotherapy is well tolerated in patients with recurrent or metastatic nonsquamous NSCLC at doses up to 9.0 μg/kg.
P1 data • Journal • Combination therapy
|
CEACAM6 (CEA Cell Adhesion Molecule 6)
|
carboplatin • pemetrexed • L-DOS47
over4years
A Dose Escalation Study of L-DOS47 in Recurrent or Metastatic Non-Squamous NSCLC (clinicaltrials.gov)
P1, N=14, Completed, Helix BioPharma Corporation | Recruiting --> Completed | N=40 --> 14 | Trial completion date: Oct 2020 --> Sep 2019 | Trial primary completion date: Oct 2020 --> Aug 2019
Clinical • Trial completion • Enrollment change • Trial completion date • Trial primary completion date • Combination therapy
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR mutation • ALK translocation
|
carboplatin • pemetrexed • L-DOS47