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DRUG CLASS:

MEK2 inhibitor

4d
A vasculogenic mimicry subtype unveiled by integrated multi-omics predicts prognosis and guides immunotherapy in MIBC. (PubMed, Front Bioinform)
Combined treatment with the MEK inhibitor TAK-733 and immune checkpoint inhibitors was proposed as a promising therapeutic strategy for this subgroup. This novel VM-based molecular subtyping system for MIBC shows strong potential for clinical application in prognosis prediction, immunotherapy response evaluation, and targeted drug discovery, providing a framework to guide personalized treatment strategies for MIBC patients.
Journal • Tumor mutational burden • IO biomarker
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TMB (Tumor Mutational Burden)
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REC-4881
2ms
New P3 trial
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gemcitabine • albumin-bound paclitaxel • atebimetinib (IMM-1-104)
2ms
A Phase 2 Study of Luvometinib Combined With Anlotinib in KRAS-mutated NSCLC (clinicaltrials.gov)
P2, N=48, Not yet recruiting, Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.
New P2 trial
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KRAS (KRAS proto-oncogene GTPase)
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KRAS mutation
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Focus V (anlotinib) • Fumaining (luvometinib)
2ms
TUPELO: Evaluate REC-4881 in Participants With Familial Adenomatous Polyposis (FAP) (clinicaltrials.gov)
P1/2, N=67, Recruiting, Recursion Pharmaceuticals Inc. | Trial completion date: Jul 2026 --> Sep 2027 | Trial primary completion date: Jul 2026 --> Jun 2027
Trial completion date • Trial primary completion date
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APC (APC Regulator Of WNT Signaling Pathway)
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REC-4881
2ms
Evaluation of TQ-B3234 Capsules in Patients With Symptomatic, Non-Surgical Type 1 Neurofibromatosis-Associated Plexiform Neurofibromas (clinicaltrials.gov)
P3, N=177, Recruiting, Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Not yet recruiting --> Recruiting
Enrollment open
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NF1 (Neurofibromin 1)
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TQ-B3234
4ms
New trial
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CD20 positive
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vincristine • prednisone • Fumaining (luvometinib) • mercaptopurine
4ms
New P3 trial
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NF1 (Neurofibromin 1)
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TQ-B3234
4ms
A Study of REC-4881 in Participants With Cancers Which Have an AXIN1 or APC Mutation (clinicaltrials.gov)
P2, N=18, Terminated, Recursion Pharmaceuticals Inc. | N=60 --> 18 | Trial completion date: Jan 2027 --> Feb 2025 | Active, not recruiting --> Terminated | Trial primary completion date: Jan 2027 --> Feb 2025; Study was terminated due to sponsor decision. This decision was not related to safety concerns.
Enrollment change • Trial completion date • Trial termination • Trial primary completion date
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APC (APC Regulator Of WNT Signaling Pathway) • RAS (Rat Sarcoma Virus) • AXIN1 (Axin 1)
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REC-4881
5ms
New P4 trial
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NF1 (Neurofibromin 1)
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Fumaining (luvometinib)
5ms
New trial
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Fumaining (luvometinib)
8ms
A single center, single arm, prospective clinical study initiated by a researcher on the efficacy and safety of FCN-159 table (ChiCTR2500109679)
P=N/A, N=20, Completed, Beijing Childrens Hospital,Capital Medical University; Beijing Childrens Hospital,Capital Medical University
New trial
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Fumaining (luvometinib)
8ms
Phase 1 Study of Luvometinib Use in Pediatric Patients with Neurofibromatosis Type 1-Related Unresectable Plexiform Neurofibromas. (PubMed, Target Oncol)
Luvometinib had a manageable safety profile in pediatric patients with unresectable NF1-related PN. Encouraging preliminary efficacy was observed, particularly among patients receiving the RP2D of 5 mg/m2, supporting further investigation of luvometinib in this setting.
P1 data • Journal
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NF1 (Neurofibromin 1)
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Fumaining (luvometinib)