Company
GSK
11 active trials that select patients by a biomarker on marked.bio, across 2 biomarkers; 5 in phase 3.
Counts only trials this company leads as sponsor, not partnered or academic trials of its drugs.
Biomarkers
Drugs in these trials
Targeted, immune and antibody-drug-conjugate therapies named in the company's active biomarker-selected trials (including other companies' drugs used in combination).
Upcoming readouts
Active phase 2 and 3 trials whose primary completion date falls in the next 12 months, according to the sponsor.
- 2026-11 A Study of Dostarlimab in Untreated dMMR/MSI-H Locally Advanced Rectal Cancer Phase 2 · MSI-H / dMMR
- 2027-01 A Study to Evaluate the Safety of Dostarlimab in Adult Participants in India With Recurrent or Advanced Endometrial Cancer (EC) Phase 4 · MSI-H / dMMR
- 2027-10 A Study of Dostarlimab in Participants With Untreated Locally Advanced Rectal Cancer in China Phase 2 · MSI-H / dMMR
Trials
11 of 37 trials shown
-
A Study to Evaluate the Safety of Dostarlimab in Adult Participants in India With Recurrent or Advanced Endometrial Cancer (EC)
dostarlimab FDA EU
Documented case of dMMR/MSI-H recurrent or advanced EC that has progressed on or following prior treatment with platinu…
MSI-H / dMMRNeoplasms, Endometrial
-
A Study to Investigate Mocertatug Rezetecan With Bevacizumab Compared With Platinum Doublet With Bevacizumab in Participants With Platinum-sensitive Ovarian Cancer (BEHOLD-Ovarian02)
Mocertatug rezetecan (Mo-Rez)carboplatinpaclitaxelgemcitabinepegylated liposomal doxorubicinbevacizumab FDA EU
…al testing (compliant to local regulations) for tumor and/or germline Breast Cancer Gene (BRCA1 and BRCA2) mutation.
BRCA1/2 mutationOvarian Neoplasms
-
A Study to Investigate Mocertatug Rezetecan Compared With Standard of Care in Participants With Platinum-resistant Ovarian Cancer (BEHOLD-Ovarian01)
Mocertatug rezetecanpaclitaxelpegylated liposomal doxorubicintopotecangemcitabinepembrolizumabbevacizumab FDA EU
PARPi, in participants with known or suspected deleterious germline or somatic BRCA mutations and who achieved a complete or partial response to platinum-based chemotherapy must have …
BRCA1/2 mutationOvarian Neoplasms
-
A Study of the Duration of Dostarlimab in Untreated Mismatch Repair Deficient (dMMR)/ Microsatellite Instability-high (MSI-H) Locally Advanced Rectal Cancer
dostarlimab FDA EU
…MR protein expression (MLH1, MSH2, MSH6, PMS2) where loss of 1 or more proteins indicates dMMR
MSI-H / dMMRNeoplasms, Rectal
-
Study of Perioperative Dostarlimab in Participants With Untreated T4N0 or Stage III dMMR/MSI-H Resectable Colon Cancer
dostarlimab FDA EUCAPEOXFOLFOX
Has a tumor demonstrating the presence of either dMMR status or MSI-H
MSI-H / dMMRColonic Neoplasms, Neoplasms, Colon
-
A Study of Dostarlimab in Combination With Carboplatin-paclitaxel in Chinese Participants With Primary Advanced or Recurrent Endometrial Cancer (EC)
dostarlimab FDA EUcarboplatinpaclitaxel
…molecular subtype of defective mismatch repair (dMMR) or microsatellite instability high (MSI-H) determined by the central reference laboratory before study intervention.
MSI-H / dMMRNeoplasms, Endometrial
-
A Study to Investigate the Safety and Preliminary Efficacy of GSK5460025 Alone or in Combination With Other Anti-cancer Agents in Participants With Solid Tumors
GSK5460025
…lt Participants With Mismatch Repair-deficient (dMMR) or Microsatellite Instability-High (MSI-H) Solid Tumors
MSI-H / dMMRNeoplasms, Colorectal, Neoplasms
-
A Study to Investigate the Safety, Pharmacokinetics, and Preliminary Effectiveness of GSK4418959 Alone or in Combination With Other Anti-cancer Agents in Participants With Solid Tumors
GSK4418959PD-1 inhibitor
…lt Participants With Mismatch Repair-deficient (dMMR) or Microsatellite Instability-High (MSI-H) Solid Tumors (SYLVER)
MSI-H / dMMRNeoplasms, Colorectal, Solid Tumor, Colon Cancer, Rectal Cancer
-
A Study of Dostarlimab in Participants With Untreated Locally Advanced Rectal Cancer in China
dostarlimab FDA EU
Participant has a tumor which can be categorized as dMMR or MSI-H by central assessment
MSI-H / dMMRNeoplasms, Rectal
-
A Study of Dostarlimab in Untreated dMMR/MSI-H Locally Advanced Rectal Cancer
dostarlimab FDA EU
Participant has a tumor which can be categorized as dMMR or MSI-H by local or central assessment
MSI-H / dMMRNeoplasms, Rectal
-
Study of TSR-042, an Anti-programmed Cell Death-1 Receptor (PD-1) Monoclonal Antibody, in Participants With Advanced Solid Tumors
dostarlimab FDA EU
…ib, ceritinib or experimental) 4) Cohort F - Participants with recurrent or advanced dMMR/MSI-H solid tumors except endometrial cancers and gastrointestinal cancers, who have received p…
MSI-H / dMMRNeoplasms
-
A Phase III Trial of Niraparib Versus Physician's Choice in HER2 Negative, Germline BRCA Mutation-positive Breast Cancer Patients
niraparib FDA EUPhysician's choice
Germline BRCA1 or BRCA2 mutation
BRCA1/2 mutationNeoplasms, Breast, Carcinoma of Breast, Human Epidermal Growth Factor 2 Negative Carcinoma of Breast, BRCA1 Gene Mutation
-
GSK1120212 vs Chemotherapy in Advanced or Metastatic BRAF V600E/K Mutation-positive Melanoma
trametinib FDA EUChemotherapy
…e (Stage IIIc) or metastatic (Stage IV) cutaneous melanoma which is also determined to be BRAF V600E/K mutation-positive by the central laboratory
BRAF V600EMelanoma
-
A Study Comparing GSK2118436 to Dacarbazine (DTIC) in Previously Untreated Subjects With BRAF Mutation Positive Advanced (Stage III) or Metastatic (Stage IV) Melanoma
dabrafenib FDA EUdacarbazine
…unresectable Stage III) or metastatic (Stage IV) melanoma that is BRAF mutation positive (V600E)
BRAF V600ECancer
-
A Study to Evaluate Foretinib in Subjects With Non-Small-Cell Lung Cancer
Foretiniberlotinib FDA EU
…the following: Evidence of Epidermal growth factor receptor activating mutation positive (EGFRm) or Epidermal growth factor receptor (EGFR)/ Wild Type (WT) genes in Deoxyribonucleic aci…
EGFR exon 19 deletion / L858RROS1 fusionCancer
-
Dabrafenib/Trametinib, BRAF or BRAF AND MEK Pre-op With BRAF and MEK Post-op, Phase IIB, Melanoma With Brain Mets,Biomarkers and Metabolites
dabrafenib FDA EUtrametinib FDA EU
Histologically-confirmed metastatic melanoma (Stage IV), carrying BRAF V600E or V600K mutation as determined by testing certified for clinical diagnostic purposes.
BRAF V600EMelanoma and Brain Metastases
-
Japan PhI/II of GSK2118436 and GSK1120212 Combination in Subjects With BRAF V600E/K Mutation Positive Advanced Solid Tumors (Phase I Part) or Cutaneous Melanoma (Phase II Part)
dabrafenib FDA EUtrametinib FDA EU
Japan PhI/II of GSK2118436 and GSK1120212 Combination in Subjects With BRAF V600E/K Mutation Positive Advanced Solid Tumors (Phase I Part) or Cutaneous Melanoma (Phase II …
BRAF V600ESolid Tumours
-
Phase II Biomarker Study Comparing the Combination of BRAF Inhibitor Dabrafenib With MEK Inhibitor Trametinib Versus the Combination After Monotherapy With Dabrafenib or Trametinib
dabrafenib FDA EUtrametinib FDA EU
BRAF (proto-oncogene B-Raf) V600E/K mutation-positive confirmed by a local laboratory.
BRAF V600EMelanoma
-
An Open-label Study of GSK1120212 Compared With Docetaxel in Stage IV KRAS-mutant Non-small Cell Lung Cancer
trametinibdocetaxel
An Open-label Study of GSK1120212 Compared With Docetaxel in Stage IV KRAS-mutant Non-small Cell Lung Cancer
KRAS G12CKRAS G12DLung Cancer, Non-Small Cell
-
A Study of GSK2118436 in BRAF Mutant Metastatic Melanoma to the Brain
dabrafenib FDA EU
Histologically confirmed metastatic melanoma (Stage IV), carrying BRAF V600E- or V600K-mutation.
BRAF V600EMelanoma and Brain Metastases
-
A Study of GSK2118436 in BRAF Mutant Metastatic Melanoma
dabrafenib FDA EU
…ically confirmed cutaneous metastatic melanoma (Stage IV) that is BRAF mutation-positive (V600 E/K) as determined via central testing with a BRAF mutation assay.
BRAF V600EMelanoma
-
Study to Determine the Effectiveness of GSK1120212 in BRAF Mutation-positive Melanoma Previously Treated With or Without a BRAF Inhibitor
trametinib FDA EU
Documented positive BRAF mutation (V600E, V600K, or V600D).
BRAF V600ECancer
-
Study Evaluating the Antitumor Activity and Safety of Niraparib as Neoadjuvant Treatment in Participants With Breast Cancer
niraparib FDA EU
…or Activity and Safety of Niraparib as Neoadjuvant Treatment in Localized, HER2-negative, BRCA-mutant Breast Cancer Patients
BRCA1/2 mutationNeoplasms, Breast
-
First Time in Humans (FTIH) Study of GSK3368715 in Participants With Solid Tumors and Diffuse Large B-cell Lymphoma (DLBCL)
GSK3368715
…nce of echinoderm microtubule-associated protein-like 4- anaplastic lymphoma kinase (EML4-ALK) rearrangement
ALK fusionNeoplasms
-
Pharmacokinetics of Repeat Oral Doses of Dabrafenib and the Combination of Dabrafenib and Trametinib in Chinese Subjects With Melanoma
dabrafenib FDA EUtrametinib FDA EU
…eous melanoma that is either Stage IIIC (unresectable) or Stage IV (metastatic), and BRAF V600E/K mutation-positive from the designated qualified laboratory for this study.
BRAF V600EMelanoma
-
Dose Escalation and Expansion Study of GSK3359609 in Participants With Selected Advanced Solid Tumors (INDUCE-1)
feladilimab (GSK3359609)GSK3174998pembrolizumab FDA EUdocetaxelpemetrexedpaclitaxelcarboplatingemcitabinefluorouracilcisplatindostarlimab FDA EUCobolimab
Microsatellite Instability-High/deficient mismatch repair (MSI-H/dMMR) tumor (Part 1B and Part 2B) and Human Papilloma Virus (HPV)-positive or Epstein-Bar…
MSI-H / dMMRNeoplasms
-
Effects of Dabrafenib on the Single Dose Pharmacokinetics (PK) of Rosuvastatin and Midazolam
Rosuvastatin10 mg tabletmidazolamdabrafenib FDA EU
BRAF V600 mutation-positive tumor: as confirmed by a Clinical Laboratory Improvement Amendments (CL…
BRAF V600ECancer
-
Study of Dabrafenib +/- Trametinib in Combination With Ipilimumab for V600E/K Mutation Positive Metastatic or Unresectable Melanoma
dabrafenib FDA EUtrametinib FDA EUipilimumab
…a that is either Stage IIIc (unresectable) or Stage IV (metastatic), and determined to be BRAF V600E or V600K mutation-positive by the local laboratory.
BRAF V600ESolid Tumours
-
A Pharmacokinetics (PK) Study of the Effects Rabeprazole and Rifampin on Dabrafenib in Subjects With BRAF V600 Mutation Positive Tumors
dabrafenib FDA EURabeprazole 40 mg once daily (OD)Rifampin 600 mg OD
BRAF V600 mutation-positive tumor as confirmed in a Clinical Laboratory Improvement Amendments (CLI…
BRAF V600ECancer
-
A Study to Evaluate the Effect of Repeat Oral Dosing of GSK2118436 on Cardiac Repolarization in Subjects With V600 BRAF Mutation-Positive Tumors
dabrafenib FDA EU
Has confirmed diagnosis of a V600 BRAF-mutation positive tumor as determined by appropriate genetic testing.
BRAF V600ECancer
-
A Phase I Study to Investigate the Safety, Tolerability and Pharmacokinetic Profile of of GSK2118436 in Japanese Subjects With BRAF Mutation Positive Solid Tumors
dabrafenib FDA EU
Subjects must have BRAF V600E or K mutant positive tumors.
BRAF V600ECancer
-
A Pharmacokinetics Study of the Effects of GSK2118436 on Warfarin, the Effects of Ketoconazole and Gemfibrozil on GSK2118436, and the Effects of Repeat Doses of GSK2118436 in Subjects With BRAF Mutant Solid Tumors
WarfarinKetoconazoleGemfibrozildabrafenib FDA EU
BRAF V600 mutation-positive tumor as determined in a CLIA-approved laboratory or equivalent (the lo…
BRAF V600ECancer
-
Determination of the Absolute Bioavailability of GSK2118436 Following a Single Oral Dose Co-Administered With an Intravenous Radiolabelled Microtracer of GSK2118436 in Subjects With BRAF Mutant Solid Tumors
dabrafenib FDA EU
BRAF mutation-positive tumor as determined via relevant genetic testing;
BRAF V600ECancer
-
An Absorption, Distribution, Metabolism and Excretion (ADME) Study of Single Oral Dose [14C] GSK2118436 in Subjects With BRAF Mutant Solid Tumors
dabrafenib FDA EU
BRAF mutation-positive tumor (V600 E/K mutation) as determined via relevant genetic testing;
BRAF V600ECancer
-
An Open Label Study to Examine the Effects of a High-Fat Meal and Particle Size on the Pharmacokinetics of Orally Administered GSK2118436 in Subjects With BRAF Mutation Positive Tumor
Regimen ARegimen BRegimen CRegimen D
BRAF mutation-positive tumor as determined via relevant genetic testing;
BRAF V600ECancer
-
A Phase I Study to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics of GSK2118436 in Subjects With Solid Tumors
dabrafenib FDA EUmidazolam
Part 2/Cohort C only: Must have BRAF positive melanoma with the V600E mutation.
BRAF V600ECancer
-
Open-label Study to Investigate the Safety, PK, and Pharmacodynamics of GSK1120212 in Subjects With Solid Tumors or Lymphoma
CRC must be KRAS or BRAF mutation positive.
KRAS G12CKRAS G12DBRAF V600ESolid Tumours
No trials match these filters.