MK-2010 for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether a new medicine, MK-2010, can treat advanced solid tumors—cancers in organs or tissues that have spread and cannot be surgically removed. Researchers aim to determine if MK-2010 alone or combined with other treatments can shrink or eliminate these tumors. Participants with visible solid tumors on scans and well-controlled HIV might be suitable for this trial. As a Phase 2 trial, this research focuses on assessing the treatment's effectiveness in an initial, smaller group of people.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that MK-2010, when used alone, has been generally safe in early studies, with most patients experiencing few serious side effects. The same applies when MK-2010 is combined with other treatments like Carboplatin, Paclitaxel, Pemetrexed, and Cisplatin, as these combinations have also proven safe in early trials.
This trial is in an early phase, focusing on the treatment's safety and patient tolerance. Researchers are still learning about possible side effects and their frequency. So far, the treatment appears promising for patients with advanced solid tumors.12345Why are researchers excited about this trial's treatments?
Researchers are excited about MK-2010 for cancer because it offers a unique approach compared to existing treatments. Unlike current therapies that often rely solely on chemotherapy, MK-2010 is an experimental drug that can be combined with various chemotherapy regimens such as Carboplatin, Paclitaxel, and others, potentially enhancing their effectiveness. Additionally, MK-2010 is explored in combination with Belzutifan, suggesting a novel mechanism of action that could target tumors more precisely. This versatility and potential for improved outcomes make MK-2010 a promising candidate in the fight against cancer.
What evidence suggests that this trial's treatments could be effective for advanced solid tumors?
Research has shown that MK-2010 aids the immune system in fighting cancer by targeting specific proteins, PD-L1 and VEGF, which cancer cells use to evade immune attacks. In other treatments focusing on these proteins, patients have experienced promising outcomes, including a 49% reduction in cancer progression and tumor shrinkage in about 35% of patients with certain cancer types. In this trial, participants may receive MK-2010 alone or with chemotherapy drugs like Carboplatin and Paclitaxel. Previous studies have found these combinations effective against hard-to-treat cancers. This suggests that MK-2010, whether used alone or with other drugs in this trial, could potentially help shrink advanced solid tumors that cannot be surgically removed.45678
Who Is on the Research Team?
Medical Director
Principal Investigator
Merck Sharp & Dohme LLC
Are You a Good Fit for This Trial?
This trial is for adults with advanced solid tumors (cancers in organs or tissues that have spread and can't be removed by surgery). Participants must have measurable cancer, good organ function, and be able to take oral medicine if needed. People with well-controlled HIV can join.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive MK-2010 as monotherapy or in combination with other treatments such as chemotherapy
Dose-Limiting Toxicity Evaluation
Participants are monitored for dose-limiting toxicities to adjust treatment doses
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- 5-Fluorouracil
- Belzutifan
- Carboplatin
- Cisplatin
- Epinephrine
- Gemcitabine
- Leucovorin or Levoleucovorin
- MK-2010
- Nab-paclitaxel
- Oxaliplatin
- Paclitaxel
- Pembrolizumab
- Pemetrexed
Trial Overview
Researchers are testing MK-2010 alone or combined with other cancer drugs like chemotherapy and immunotherapy. The study aims to see how safe these treatments are and whether they help shrink or control the cancer.
How Is the Trial Designed?
7
Treatment groups
Experimental Treatment
Active Control
Participants receive MK-2010 intravenously as monotherapy.
Participants receive MK-2010 intravenously in combination with Pemetrexed and either Cisplatin or Carboplatin chemotherapy.
Participants receive MK-2010 intravenously in combination with Gemcitabine and Cisplatin chemotherapy.
Participants receive MK-2010 intravenously in combination with FOLFOX chemotherapy (comprising Leucovorin or Levoleucovorin, 5-Fluorouracil, and Oxaliplatin).
Participants receive MK-2010 intravenously in combination with Carboplatin and either Paclitaxel or Nab-paclitaxel chemotherapy.
Participants receive MK-2010 intravenously in combination with oral Belzutifan.
Participants receive Pembrolizumab intravenously in combination with FOLFOX chemotherapy (comprising Leucovorin or Levoleucovorin, 5-Fluorouracil, and Oxaliplatin).
Find a Clinic Near You
Who Is Running the Clinical Trial?
Merck Sharp & Dohme LLC
Lead Sponsor
Chirfi Guindo
Merck Sharp & Dohme LLC
Chief Marketing Officer since 2022
Degree in Engineering from Ecole Centrale de Paris, MBA from New York University Stern School of Business
Robert M. Davis
Merck Sharp & Dohme LLC
Chief Executive Officer since 2021
JD from Northwestern University Pritzker School of Law, MBA from Northwestern University Kellogg Graduate School of Management, Bachelor's in Finance from Miami University
Citations
Therapeutic Targeting of VEGFR-2, PD-L1, and EGFR–MET ...
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3.
onclive.com
onclive.com/view/imm2510-induces-early-efficacy-in-advanced-immunotherapy-exposed-squamous-nsclcIMM2510 Induces Early Efficacy in Advanced, ... - OncLive
The median progression-free survival was 9.4 months (95% CI, 1.87-NA). “Based on these findings, a phase 2 study evaluating IMM2510 in ...
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biocytogen.com
biocytogen.com/blogs/humanized-mouse-model-pd1-vegf-dual-targeting-a-potent-one-two-punch-in-cancer-therapyPD-1 × VEGF Dual Targeting: A Potent One-Two Punch in ...
In PD-L1–positive, treatment-naïve non-small cell lung cancer (NSCLC) patients, AK112 reduced the risk of disease progression by 49% compared to ...
5.
friendsofcancerresearch.org
friendsofcancerresearch.org/wp-content/uploads/Panel-4-Large-treatment-effects-issue-brief-11-2-11.pdfPanel-4-Large-treatment-effects-issue-brief- ...
Overall survival was the primary efficacy endpoint. Given the impressive Phase 1 and Phase 2 results (response rates of > 50% in the targeted population of.
6.
trial.medpath.com
trial.medpath.com/news/lanova-medicines-announces-initiation-of-phase-1-clinical-trial-of-anti-pd-1-vegf-biospaceLaNova Medicines Initiates Phase 1 Trial of LM-299, Anti- ...
Preclinical studies of LM-299View drug details demonstrated strong inhibition of tumor growth and a favorable safety profile, supporting its ...
P3.12: IMM2510, an Anti-PD-L1/VEGF Bispecific Antibody ...
[3,4]. • Here, we present preliminary efficacy and safety data of IMM2510 in advanced squamous non-small- cell lung cancer (sq-NSCLC) patients (pts) from phase ...
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