Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

OVV-01 Intravenous and Intratumoral Injection Combined With AK112 for the Treatment of Advanced Solid Tumors

sunnuntai 14. kesäkuuta 2026 päivittänyt: Cancer Institute and Hospital, Chinese Academy of Medical Sciences

A Single-Arm, Open-Label Clinical Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of OVV-01 Administered Intravenously and Intratumorally in Combination With AK112 in Patients With Advanced Solid Tumors

This study is an open-label, multiple-route-of-administration dose-escalation clinical trial designed to evaluate the safety and preliminary efficacy of OVV-01 injection administered intravenously or intravenously plus intratumorally, either as monotherapy or in combination with AK112 injection, in subjects with advanced solid tumors.

Tutkimuksen yleiskatsaus

Tila

Ei vielä rekrytointia

Yksityiskohtainen kuvaus

Eligible subjects must have advanced malignant solid tumours that have been confirmed by histology or cytology and possess measurable, injectable tumour lesions, including superficial and deep lesions that can be injected under ultrasound/CT guidance.

The study comprises a screening period, a treatment period and a follow-up period. The screening period runs from the day the subject signs the ICF (Day -28) until the day before the first dose is administered (Day -1). Eligible subjects will receive intravenous (IV) therapy alone or in combination with AK112 (Part 1), or IV therapy plus intratumoral (IT) therapy alone or in combination with AK112 (Part 2). Dosing occurs on Days 1 and 3 (D1 and D3) of each two-week treatment cycle, for up to six cycles. IV and IT injections are administered on the same day. If a DLT occurs during the DLT observation period, OVV-01 administration will be discontinued. Treatment will continue until disease progression occurs, the subject develops intolerable toxicity, the subject withdraws informed consent, the subject dies or is lost to follow-up, the investigator determines that termination is in the subject's best interests, or the subject completes six consecutive cycles, whichever occurs first.

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

30

Vaihe

  • Vaihe 1

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Tutki yhteystietojen varmuuskopiointi

Opiskelupaikat

    • Langfang
      • Hebei, Langfang, Kiina
        • Cancer Hospital Chinese Academy of Medical Sciences

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Ei

Kuvaus

Inclusion Criteria:

  1. At least 18 years of age at the time of signing the ICF; gender is not restricted.
  2. Patients with advanced solid tumors confirmed by histopathological/cytological examination of the primary and/or metastatic lesions, including but not limited to: melanoma, head and neck squamous cell carcinoma, cervical cancer, osteosarcoma, nasopharyngeal carcinoma, breast cancer, lung cancer, colorectal cancer, hepatocellular carcinoma, gastric cancer, etc.
  3. Patients with advanced disease who have failed standard therapy, lack standard treatment options, or are medically ineligible for standard therapy. Patients must have progressed after receiving at least two standard therapies (including but not limited to targeted therapies).
  4. Subjects must have at least one measurable lesion as defined by RECIST 1.1 criteria, i.e., non-lymph node lesions ≥10 mm in longest diameter and lymph node lesions ≥15 mm in shortest diameter on CT or MRI. Injectable tumor lesions must be present, including superficial lesions and deep lesions amenable to injection under ultrasound/CT/or endoscopic guidance.
  5. ECOG performance status of 0-1, with an estimated survival of at least 12 weeks.
  6. Sufficient organ and hematopoietic function.
  7. Women of childbearing potential must have a negative pregnancy test within 7 days prior to treatment initiation.
  8. Male and female subjects of childbearing potential must agree to use reliable contraception during the trial and for at least 6 months after the last dose.

Exclusion Criteria:

  1. Patients with known brain metastases and/or clinically suspected brain metastases (however, patients with asymptomatic brain metastases or those clinically stable for over 3 months following local treatment may be enrolled);
  2. Subjects who underwent radiotherapy to the target lesion within the past 2 months (may be enrolled if the radiotherapy site progressed);
  3. Subjects with other active malignancies within the past 5 years. Exceptions include subjects who have achieved complete remission and require no follow-up treatment, or subjects with malignancies within the scope of the indication;
  4. Largest diameter of lesions for injection >100 mm;
  5. Subjects who have participated in or are currently participating in other drug or medical device clinical trials within the past 4 weeks;
  6. Subjects scheduled for or who have previously undergone tissue/organ transplantation;
  7. Subjects with Human Immunodeficiency Virus (HIV) infection who have experienced AIDS-related opportunistic infections within the past 12 months, or who have a CD4+ T-cell (CD4+) count < 350 cells/uL; Patients screening positive for hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HBcAb) with HBV-DNA above the lower limit of detection, or screening positive for HCV antibody with HCV-RNA above the lower limit of detection; subjects with positive syphilis serology;
  8. Subjects requiring antiviral therapy during the study period or within 5 half-lives of the first dose of antiviral therapy.
  9. Subjects requiring therapeutic anticoagulant therapy during the study period.
  10. Subjects with uncontrolled active infection ≥ Grade 3 according to CTCAE v5.0 that is clinically significant;
  11. Received antineoplastic therapy (chemotherapy, radiotherapy, biologic therapy, endocrine therapy, immunotherapy, etc.) within 4 weeks prior to first dose; Received small-molecule targeted therapy or oral fluorouracil-based agents within 2 weeks prior to first dose or within 5 half-lives (whichever is longer); Received Chinese herbal medicine or proprietary Chinese medicine with antitumor indications within 2 weeks prior to the first dose; Received nitrosourea or mitomycin C within 6 weeks prior to the first dose; Palliative radiotherapy for non-target lesions is permitted (≥2 weeks prior to the first dose);

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Ei satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Ei mitään (avoin tarra)

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: OVV-01 intravenous injection
OVV-01 injection is administered on Day 1 and Day 3 (D1, D3) of each cycle, with a 2-week treatment cycle lasting up to 6 cycles; Upon enrollment of 3 subjects in the OVV-01 monotherapy intravenous group with no DLT events, the combination therapy group may be initiated; In the combination therapy group, OVV-01 injection is administered on Day 1 and Day 3 (D1, D3) of each cycle, while AK112 is administered on Day 1 (D1) of each cycle. Each treatment cycle spans 2 weeks, with a maximum of 6 cycles administered.
OVV-01 is administered twice every two weeks
AK112 is administered once every two weeks.
Kokeellinen: OVV-01 IV + IT

OVV-01 injection is administered on Day 1 and Day 3 (D1, D3) of each cycle, with a 2-week treatment cycle lasting up to 6 cycles; intratumoral injection and intravenous injection are completed on the same day.

The OVV-01 monotherapy intravenous group may initiate the combination therapy group once 3 subjects are enrolled and no DLT events occur.

For the combination therapy group: OVV-01 injection is administered on Day 1 and Day 3 (D1, D3) of each cycle, while AK112 is administered on Day 1 (D1) of each cycle. Each treatment cycle spans 2 weeks, with a maximum of 6 cycles administered. Intratumoral injection and intravenous injection are completed on the same day.

OVV-01 is administered twice every two weeks
AK112 is administered once every two weeks.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Haittatapahtumien (AEs) ilmaantuvuus
Aikaikkuna: ICF:n allekirjoittamisesta aina 24 kuukautta viimeisen infuusion jälkeen.
Hoidon aikana esiintyvien haittatapahtumien (TEAE) esiintyvyys ja vakavuus NCI CTCAE v5.0:n mukaisesti luokiteltuna.
ICF:n allekirjoittamisesta aina 24 kuukautta viimeisen infuusion jälkeen.
DLT
Aikaikkuna: Within 21 days after administration
According to the internationally accepted CTCAE v5.0 toxicity grading criteria, DLT in this study is defined as a toxicity reaction related to the study drug OVV-01 occurring within 3 weeks after the first dose.
Within 21 days after administration

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
ORR
Aikaikkuna: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
The proportion of subjects achieving CR or PR will be assessed according to RECIST 1.1.
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
DCR
Aikaikkuna: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
The proportion of subjects achieving CR, PR, or SD will be assessed according to RECIST 1.1.
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
DoR
Aikaikkuna: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
Assessment will be conducted according to RECIST 1.1. For subjects achieving objective response, DOR is defined as the time from the first documented objective tumor response (CR or PR) to the first documented disease progression or death from any cause, whichever occurs first.
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
PFS
Aikaikkuna: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
The time from the first study treatment to the first documented disease progression or death from any cause (whichever occurs first) will be assessed according to RECIST 1.1.
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
OS
Aikaikkuna: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
The time from the first study treatment to death from any cause will be assessed according to RECIST 1.1.
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Tutkijat

  • Opintojen puheenjohtaja: Ning Li, Chief, Office of Clinical Trial Center, CancerIHCAMS

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Arvioitu)

Lauantai 1. elokuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Sunnuntai 31. tammikuuta 2027

Opintojen valmistuminen (Arvioitu)

Sunnuntai 31. tammikuuta 2027

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Lauantai 28. maaliskuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Sunnuntai 14. kesäkuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Tiistai 16. kesäkuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Tiistai 16. kesäkuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Sunnuntai 14. kesäkuuta 2026

Viimeksi vahvistettu

Maanantai 1. kesäkuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • OVV-01A07

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

EI

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Tilaa