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Monoclonal Antibodies

OMTX705 + Pembrolizumab for Cancer

Phase 1
Recruiting
Research Sponsored by Oncomatryx Biopharma S.L.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 24 months
Awards & highlights

Summary

This trial tests a new drug, OMTX705, alone or with pembrolizumab, in patients with advanced cancer who have no other treatment options. The study aims to find the safest dose and see if the combination works better than OMTX705 alone.

Who is the study for?
Adults with advanced or metastatic solid tumors without standard treatment options can join this trial. They must have measurable disease, good organ function, and an ECOG performance status of 0-1. Women who can bear children and men with partners who can must use contraception. Exclusions include active infections, certain heart conditions, pregnancy, recent other cancer treatments, uncontrolled brain metastases, and specific medication interactions.
What is being tested?
OMTX705 is being tested alone and combined with Pembrolizumab to treat advanced cancers in patients lacking other options. This Phase 1 study will gradually increase doses to find safe levels (dose-escalation) before expanding the number of participants at those levels (expansion phase).
What are the potential side effects?
Possible side effects may include reactions related to the immune system such as inflammation in various organs due to OMTX705 or Pembrolizumab's action on the body's defenses. Other common drug-related issues could be fatigue, digestive problems or changes in blood counts.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 24 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Safety evaluation of OMTX705
Secondary study objectives
Evaluation of OMTX705 Immunogenicity
Evaluation of the OMTX705 Pharmacokinetics
Exercise, Aerobic
Other study objectives
Evaluation of OMTX705 biomarkers
Evaluation of OMTX705 payload metabolites
Evaluation of QTc prolongation
+3 more

Side effects data

From 2022 Phase 1 & 2 trial • 35 Patients • NCT03003468
40%
FATIGUE
37%
INFUSION RELATED REACTION
37%
NAUSEA
23%
DIARRHEA
23%
BACK PAIN
23%
ABDOMINAL PAIN
23%
ANOREXIA
20%
COUGH
20%
ARTHRALGIA
20%
NON-CARDIAC CHEST PAIN
17%
DYSPNEA
17%
CONSTIPATION
17%
CHILLS
17%
MYALGIA
13%
DIZZINESS
13%
HEADACHE
13%
PRURITUS
13%
RASH MACULO-PAPULAR
10%
ANEMIA
10%
URTICARIA
10%
SINUS TACHYCARDIA
10%
RESPIRATORY, THORACIC AND MEDIASTINAL DISORDERS - OTHER, SPECIFY
10%
EDEMA LIMBS
10%
ALLERGIC REACTION
10%
ANXIETY
10%
LUNG INFECTION
10%
SKIN AND SUBCUTANEOUS TISSUE DISORDERS - OTHER, SPECIFY
7%
EAR AND LABYRINTH DISORDERS - OTHER, SPECIFY
7%
HYPERGLYCEMIA
7%
PAIN
7%
PELVIC PAIN
7%
PRODUCTIVE COUGH
7%
PLEURAL EFFUSION
7%
VOICE ALTERATION
7%
VOMITING
7%
FEVER
7%
FLATULENCE
7%
TUMOR PAIN
7%
CREATININE INCREASED
7%
HYPERTHYROIDISM
7%
NECK PAIN
7%
DEPRESSION
7%
FLU LIKE SYMPTOMS
7%
LYMPHOCYTE COUNT DECREASED
7%
DYSPEPSIA
7%
FLUSHING
7%
HYPONATREMIA
7%
HYPOTHYROIDISM
7%
URINARY TRACT INFECTION
3%
ALKALINE PHOSPHATASE INCREASED
3%
DYSPHAGIA
3%
ESOPHAGITIS
3%
GASTROESOPHAGEAL REFLUX DISEASE
3%
OSTEONECROSIS OF JAW
3%
BRONCHOSPASM
3%
PNEUMONITIS
3%
SORE THROAT
3%
BLURRED VISION
3%
GAIT DISTURBANCE
3%
HEMORRHOIDS
3%
POSTNASAL DRIP
3%
PRESYNCOPE
3%
ACUTE KIDNEY INJURY
3%
PERIPHERAL MOTOR NEUROPATHY
3%
DRY SKIN
3%
FLASHING LIGHTS
3%
HYPOMAGNESEMIA
3%
MUSCLE WEAKNESS LOWER LIMB
3%
HYPERTENSION
3%
HYPOTENSION
3%
SINUSITIS
3%
SYNCOPE
3%
HEARING IMPAIRED
3%
RASH ACNEIFORM
3%
SOMNOLENCE
3%
COLITIS
3%
HOT FLASHES
3%
RESPIRATORY FAILURE
3%
CONJUNCTIVITIS
3%
MOVEMENTS INVOLUNTARY
3%
NASAL CONGESTION
3%
PARESTHESIA
3%
VAGINAL INFECTION
3%
GASTROINTESTINAL DISORDERS - OTHER, SPECIFY
3%
NEUTROPHIL COUNT DECREASED
3%
ALLERGIC RHINITIS
3%
PAIN IN EXTREMITY
3%
SEPSIS
3%
BLOATING
3%
DEHYDRATION
3%
DRY MOUTH
3%
INSOMNIA
3%
MALAISE
3%
PAIN OF SKIN
3%
THROMBOEMBOLIC EVENT
3%
TREMOR
3%
WEIGHT GAIN
100%
80%
60%
40%
20%
0%
Study treatment Arm
Imprime PGG 4 mg/kg
Imprime PGG 2 mg/kg

Trial Design

2Treatment groups
Experimental Treatment
Group I: Monotherapy (OMTX705)Experimental Treatment1 Intervention
OMTX705 is administered as single agent.
Group II: Combination (OMTX705 + pembrolizumab)Experimental Treatment2 Interventions
OMTX705 is administered in combination with pembrolizumab.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Pembrolizumab
2017
Completed Phase 2
~2070

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Pembrolizumab, a PD-1 inhibitor, enhances the immune system's ability to detect and destroy cancer cells by blocking the PD-1 pathway, which tumors often exploit to evade immune detection. This is particularly important for solid tumor patients as it can lead to better tumor control and improved survival rates. Other treatments like chemotherapy target rapidly dividing cells, and targeted therapies focus on specific genetic mutations within the tumor, offering a more personalized approach to cancer treatment. Understanding these mechanisms allows for more effective and tailored treatment strategies for patients with solid tumors.
Recurrent glioma clinical trial, CheckMate-143: the game is not over yet.New therapeutic strategies for malignant pleural mesothelioma.

Find a Location

Who is running the clinical trial?

Oncomatryx Biopharma S.L.Lead Sponsor
Ignacio García-Ribas, MDStudy DirectorOncomatryx Biopharm, S.L.

Media Library

OMTX705 (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05547321 — Phase 1
Solid Tumors Research Study Groups: Monotherapy (OMTX705), Combination (OMTX705 + pembrolizumab)
Solid Tumors Clinical Trial 2023: OMTX705 Highlights & Side Effects. Trial Name: NCT05547321 — Phase 1
OMTX705 (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05547321 — Phase 1
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